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33662-58-7

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33662-58-7 Usage

General Description

Methyl 2,4-dihydroxy-3-methylbenzoate is a chemical compound commonly used in various industries, including pharmaceuticals, cosmetics, and fragrances. It is a derivative of salicylic acid and is known for its anti-inflammatory and antioxidant properties, making it useful in skincare products and topical treatments for various skin conditions. Additionally, it is also used as a flavoring agent in food products and as a precursor in the synthesis of other organic compounds. The compound is typically synthesized through esterification of 2,4-dihydroxy-3-methylbenzoic acid with methanol, and it is known for its mild, sweet aroma and high stability.

Check Digit Verification of cas no

The CAS Registry Mumber 33662-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,6 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33662-58:
(7*3)+(6*3)+(5*6)+(4*6)+(3*2)+(2*5)+(1*8)=117
117 % 10 = 7
So 33662-58-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O4/c1-5-7(10)4-3-6(8(5)11)9(12)13-2/h3-4,10-11H,1-2H3

33662-58-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2,4-dihydroxy-3-methylbenzoate

1.2 Other means of identification

Product number -
Other names Methyl-3-methyl-2.4-dihydroxybenzoat

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:33662-58-7 SDS

33662-58-7Relevant articles and documents

Synthesis of isothiochroman 2,2-dioxide and 1,2-benzooxathiin 2,2- dioxide gyrase B inhibitors

Peixoto, Christophe,Laurin, Patrick,Klich, Michel,Dupuis-Hamelin, Claudine,Mauvais, Pascale,Lassaigne, Patrice,Bonnefoy, Alain,Musicki, Branislav

, p. 1741 - 1745 (2007/10/03)

The design, synthesis and in vitro biological evaluation of isothiochroman 2,2-dioxide and 1,2-benzooxathiin 2,2-dioxide analogues of coumarin inhibitors of gyrase B are described. Compared to coumarin derivatives, compounds of the 1,2-benzooxathiin 2,2-dioxide series display improved inhibitory potency in negative supercoiling of relaxed DNA gyrase. (C) 2000 Elsevier Science Ltd.

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