Category: 323579-00-6

323579-00-6, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 2-Methyl-5-chloro-6-benzoxazolamine, cas is 323579-00-6,the benzoxazole compound, it is a common compound, a new synthetic route is introduced below.

6-Amino-5,7-Dichloro-2-Methylbenzoxazole (4) 6-Amino-5-chloro-2-methylbenzoxazole (10 g, 54.76 mMole) was dissolved in ethyl acetate (150 mL). At room temperature and with good stirring, sulfuryl chloride (8.8 mL, 109.52 mMole) was added drop by drop over a 20-minute period. As the addition proceeds, additional ethyl acetate (350 mL) was added to keep the mixture stirring. After 1 hour the precipitate was filtered off, washed with ether and air-dried. Yield 10.5 g.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of 323579-00-6, 2-Methyl-5-chloro-6-benzoxazolamine

Reference：
Patent; Eastman Kodak Company; US2005/101784; (2005); A1;,
Benzoxazole – Wikipedia
Benzoxazole | C7H5NO – PubChem

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Recommanded Product: 2-Methyl-5-chloro-6-benzoxazolamine, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 323579-00-6, Name is 2-Methyl-5-chloro-6-benzoxazolamine, molecular formula is C8H7ClN2O

Photographic element, compound, and process

Disclosed is a photographic element comprising a light-sensitive silver halide emulsion layer having associated therewith a cyan ?NB coupler? having the formula (I): 1wherein the term ?NB coupler? represents a coupler of formula (I) that forms a dye for which the left bandwidth (LBW) using spin-coating is at least 5 nm less than that of the same dye in solution form; Y is H or a coupling-off group; each Z? and Z* is an independently selected substituent group where n is 0 to 4 and p is 0 to 2; W2 represents the atoms necessary to complete a heterocyclic ring group; and V is a sulfone or sulfoxide containing group; provided that the combined sum of the aliphatic carbon atoms in V, all Z? and all Z* is at least 8. The element exhibits improved cyan dye hue.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Recommanded Product: 2-Methyl-5-chloro-6-benzoxazolamine, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 323579-00-6, in my other articles.

Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem

Chemistry is traditionally divided into organic and inorganic chemistry. Computed Properties of C8H7ClN2O, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent£¬Which mentioned a new discovery about 323579-00-6

Photographic element, compound, and process

Disclosed is a photographic element comprising a light-sensitive silver halide emulsion layer having associated therewith a “NB coupler” having the formula (I):wherein :the term “NB coupler” represents a coupler of formula (I) that forms a dye for which the left bandwidth (LBW) using spin-coating is at least 5nm less than that of the same dye in solution form;Y is H or a coupling-off group;each Z* is an independently selected substituent group where p is 0 to 2;V is a substituent group containing a sulfone group;R4is represented by the formulawherein each of R5, R6and R7is hydrogen or an independently selected substituent with no more than one being hydrogen;, provided that two or more of R5, R6and R7may join to form a ring or rings and provided that the combined sum of the aliphatic carbon atoms in V, R4and all Z* is at least 8, and provided further that R4is not a fully fluorinated alkyl group. Such elements provide improved hue.

If you are interested in 323579-00-6, you can contact me at any time and look forward to more communication. Computed Properties of C8H7ClN2O

Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem

Application of 323579-00-6, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.323579-00-6, Name is 2-Methyl-5-chloro-6-benzoxazolamine, molecular formula is C8H7ClN2O. In a article£¬once mentioned of 323579-00-6

Compounds and synthesis process

Disclosed is a process for preparing a 6-chloro-2,5-dicarbonamido phenol compounds comprising a step employing a 2-alkyl-6-aminobenzoxazole to form a 2-alkyl-6-amino-7-chlorobenzoxazole in which the 2-alkyl group is unbranched at the alpha carbon. It also provides intermediate compounds useful in the process. The process provides a simple and safe way to prepare 6-chloro-2,5-dicarbonamido phenol compounds in good yield.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 323579-00-6

Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem

Application of 323579-00-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.323579-00-6, Name is 2-Methyl-5-chloro-6-benzoxazolamine, molecular formula is C8H7ClN2O. In a Patent£¬once mentioned of 323579-00-6

Photographic element, compound, and process

Disclosed is a photographic element comprising a light-sensitive silver halide emulsion layer having associated therewith a cyan coupler having the formula:wherein:V is a sulfone or sulfoxide containing group;Y is H or a coupling-off group;W2represents the atoms necessary to complete a carbocyclic or heterocyclic ring group;each Z”, Z* and Z#is an independently selected substituent group where n and r are independently 0 to 4 and p is 0 to 2; andX is a halogen atom, and s is 1 to 5;provided that the combined sum of the aliphatic carbon atoms in V, all Z”, all Z#, and all Z* is at least 8. The element exhibits improved cyan dye stability.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 323579-00-6

Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem

323579-00-6, Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent£¬Which mentioned a new discovery about 323579-00-6

Photographic element, compound, and process

Disclosed is a photographic element comprising a light-sensitive silver halide emulsion layer having associated therewith a cyan “NB coupler” having the formula (I):wherein :the term “NB coupler” represents a coupler of formula (I) that forms a dye for which the left bandwidth (LBW) using spin-coating is at least 5nm less than that of the same dye in solution form;Y is H or a coupling-off group;each Z” and Z* is an independently selected substituent group where n is 1 to 4 and p is 0 to 2;W2represents the atoms necessary to complete a carbocyclic or heterocyclic ring group; andV is a sulfone or sulfoxide containing group;provided that the combined sum of the aliphatic carbon atoms in V, all Z” and all Z* is at least 8;provided further that there is one and only one Z” substituent ortho to the carbonamido group linking the W2ring to the rest of the coupler; andprovided still further that when W2forms a carbocyclic aromatic ring, at least one Z” is selected from the group consisting of alkyl, alkoxy, hydroxy, aryl, aryloxy, oxycarbonyl, oxysulfonyl, sulfoxide, sulfamoyl, thio, carbamoyl, carboxy, carbonamido, ureido, cyano, nitro, and halogen groups. The element exhibits improved cyan dye hue.

323579-00-6, Interested yet? Read on for other articles about 323579-00-6!

Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem

It is a common heterocyclic compound, the benzoxazole compound, 2-Methyl-5-chloro-6-benzoxazolamine, cas is 323579-00-6 its synthesis route is as follows.,323579-00-6

6-Amino-5,7-Dichloro-2-Methylbenzoxazole (4) 6-Amino-5-chloro-2-methylbenzoxazole (10 g, 54.76 mMole) was dissolved in ethyl acetate (150 mL). At room temperature and with good stirring, sulfuryl chloride (8.8 mL, 109.52 mMole) was added drop by drop over a 20-minute period. As the addition proceeds, additional ethyl acetate (350 mL) was added to keep the mixture stirring. After 1 hour the precipitate was filtered off, washed with ether and air-dried. Yield 10.5 g.

With the complex challenges of chemical substances, we look forward to future research findings about 2-Methyl-5-chloro-6-benzoxazolamine

Reference£º
Patent; Eastman Kodak Company; US2005/101784; (2005); A1;,
Benzoxazole – Wikipedia
Benzoxazole | C7H5NO – PubChem

323579-00-6, 2-Methyl-5-chloro-6-benzoxazolamine is a benzoxazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

6-Amino-5,7-Dichloro-2-Methylbenzoxazole (4) 6-Amino-5-chloro-2-methylbenzoxazole (10 g, 54.76 mMole) was dissolved in ethyl acetate (150 mL). At room temperature and with good stirring, sulfuryl chloride (8.8 mL, 109.52 mMole) was added drop by drop over a 20-minute period. As the addition proceeds, additional ethyl acetate (350 mL) was added to keep the mixture stirring. After 1 hour the precipitate was filtered off, washed with ether and air-dried. Yield 10.5 g.

323579-00-6, The synthetic route of 323579-00-6 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Eastman Kodak Company; US2005/101784; (2005); A1;,
Benzoxazole – Wikipedia
Benzoxazole | C7H5NO – PubChem