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CAS

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153203-53-3

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153203-53-3 Usage

General Description

3-CHLORO-5-METHYL-BENZOIC ACID METHYL ESTER is a chemical compound that belongs to the benzene and substituted derivatives class. It is a methyl ester of 3-chloro-5-methylbenzoic acid and is often used in the manufacturing of pharmaceuticals, agrochemicals, and other organic compounds. It is a colorless, crystalline solid with a characteristic odor, and it is soluble in organic solvents such as ethanol and ether. 3-CHLORO-5-METHYL-BENZOIC ACID METHYL ESTER is also known for its mild irritant properties and should be handled with care.

Check Digit Verification of cas no

The CAS Registry Mumber 153203-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,2,0 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 153203-53:
(8*1)+(7*5)+(6*3)+(5*2)+(4*0)+(3*3)+(2*5)+(1*3)=93
93 % 10 = 3
So 153203-53-3 is a valid CAS Registry Number.

153203-53-3Relevant articles and documents

HETEROARYL-TRIAZOLE COMPOUNDS AS PESTICIDES

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Page/Page column 147-148, (2021/08/27)

The present invention relates to novel heteroaryl-triazole compounds of the general formula (I), in which the structural elements X, Y, R1, R2, R3a, R3b, R4 and R5 have the meaning given in the description, to formulations and compositions comprising such compounds and for their use in the control of animal pests including arthropods and insects in plant protection and to their use for control of ectoparasites on animals.

Meta halogenation of 1,3-disubstituted arenes via iridium-catalyzed arene borylation

Murphy, Jaclyn M.,Liao, Xuebin,Hartwig, John F.

, p. 15434 - 15435 (2008/09/19)

We report the meta halogenation of 1,3-disubstituted arenes to form 3,5-disubstituted aryl bromides and chlorides by using iridium-catalyzed arene borylation chemistry. Iridium-catalyzed borylation of arenes with B2pin2, followed by reaction of the boronic ester with copper(II) bromide or chloride converts arylboronic esters to the corresponding aryl halides. A variety of arenes containing alkoxy, alkyl, halogen, nitrile, ester, amide, and pivaloyl and TIPS-protected alcohols were converted to the corresponding 3,5-disubstituted aryl bromides and chlorides in yields ranging from 46% to 85%. In addition, 2,6-disubstituted and 3-substituted pyridines were converted to the 4-halo and 5-halopyridines, respectively. The utility of this methodology was demonstrated by the formal conversion of nicotine to Altinicline in three steps with an overall yield of 61% using meta bromination of nicotine as the first step. Copyright

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