133357-62-7 Usage
Uses
Used in Organic Synthesis:
METHYL-3-BROMOMETHYL-5-METHOXYBENZOATE is used as a building block for the synthesis of various organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, METHYL-3-BROMOMETHYL-5-METHOXYBENZOATE is utilized as a key intermediate in the production of pharmaceuticals, aiding in the discovery and development of novel drugs with potential therapeutic benefits.
Used in Biological and Medicinal Studies:
METHYL-3-BROMOMETHYL-5-METHOXYBENZOATE is employed in research to explore its potential biological and medicinal properties, with the aim of identifying new therapeutic agents or understanding its interactions with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 133357-62-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,5 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133357-62:
(8*1)+(7*3)+(6*3)+(5*3)+(4*5)+(3*7)+(2*6)+(1*2)=117
117 % 10 = 7
So 133357-62-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H11BrO3/c1-13-9-4-7(6-11)3-8(5-9)10(12)14-2/h3-5H,6H2,1-2H3
133357-62-7Relevant articles and documents
HEDGEHOG ANTAGONISTS HAVING ZINC BINDING MOIETIES
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Paragraph 0162; 0250, (2014/02/16)
The present invention provides compounds which antagonize hedgehog signaling and inhibit HDAC activity. The com-pounds can be used in methods of treating proliferative dis-eases and disorders such as cancer
BIFUNCTIONAL CHELATING AGENTS
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Page/Page column 103-104, (2011/09/19)
A bifunctional chelating agent of the formula (I): wherein the variables R1, R1 , Q1, Q2 and M are as defined in the description of the present application. Also described is a complex of the above chelating age
A concise total synthesis of the aglycone of the gilvocarcins
Deshpande, Prashant P.,Martin, Olivier R.
, p. 6313 - 6316 (2007/10/02)
A brief and convergent synthesis of the aglycone of the gilvocarcins M and E (and formally V) involving, in the key step, a Pd-mediated intramolecular biaryl coupling, is reported.
