876746-33-7 Usage
Description
Methyl 3-(3-chloro-2,4-dihydroxyphenyl)propanoate is a chemical compound that belongs to the class of methyl esters. It is composed of a methyl group attached to a propanoate chain, which is in turn connected to a 3-(3-chloro-2,4-dihydroxyphenyl) group. Methyl 3-(3-chloro-2,4-dihydroxyphenyl)propanoate is synthesizable and is commonly used in organic chemistry and pharmaceutical research. The presence of the chloro and hydroxy groups in its phenyl moiety indicates its potential reactivity and biological activity.
Uses
Used in Pharmaceutical Research:
Methyl 3-(3-chloro-2,4-dihydroxyphenyl)propanoate is used as an intermediate in the synthesis of various pharmaceutical compounds for its potential reactivity and biological activity.
Used in Organic Chemistry:
Methyl 3-(3-chloro-2,4-dihydroxyphenyl)propanoate is used as a reagent in various organic chemical reactions due to its potential reactivity.
Used in Chemical and Industrial Processes:
Methyl 3-(3-chloro-2,4-dihydroxyphenyl)propanoate may have potential applications in other chemical and industrial processes, although specific uses are not detailed in the provided materials.
It is important to handle Methyl 3-(3-chloro-2,4-dihydroxyphenyl)propanoate with care and follow proper safety procedures due to its potential hazards and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 876746-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,7,4 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 876746-33:
(8*8)+(7*7)+(6*6)+(5*7)+(4*4)+(3*6)+(2*3)+(1*3)=227
227 % 10 = 7
So 876746-33-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO4/c1-15-8(13)5-3-6-2-4-7(12)9(11)10(6)14/h2,4,12,14H,3,5H2,1H3
876746-33-7Relevant articles and documents
Mild synthesis of asymmetric 2′-carboxyethyl-substituted fluoresceins
Lukhtanov, Eugeny A.,Vorobiev, Alexei V.
, p. 2424 - 2427 (2008/09/19)
(Chemical Equation Presented) Asymmetric fluoresceins bearing a carboxyethyl group in the chromophoric portion of the dyes were prepared by a reaction of substituted phthalic anhydride with a carboxyethyl substituted resorcinol analogue followed by a condensation with a second resorcinol analogue. In order to avoid an accumulation of symmetric side products, the second step was performed in two substeps: acid-catalyzed formation of a triphenylmethyl intermediate followed by base-catalyzed cyclization which furnished the desired dyes.
