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74733-27-0

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74733-27-0 Usage

General Description

Methyl 4-(bromomethyl)-2-methoxybenzoate is a chemical compound that falls under the category of esters and benzene derivatives. It is comprised of a methyl group, a bromomethyl group, and a methoxy group attached to a benzene ring. methyl 4-(bromomethyl)-2-methoxybenzoate is used in organic synthesis and is commonly employed in the pharmaceutical industry for the production of various medications and drugs. Its unique chemical structure makes it useful for the development of new compounds and substances with potential therapeutic properties. However, the compound should be handled and stored with care, as it may pose health and safety hazards if not managed properly. Overall, methyl 4-(bromomethyl)-2-methoxybenzoate plays a critical role in the advancement of pharmaceutical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 74733-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,3 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74733-27:
(7*7)+(6*4)+(5*7)+(4*3)+(3*3)+(2*2)+(1*7)=140
140 % 10 = 0
So 74733-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H11BrO3/c1-13-9-5-7(6-11)3-4-8(9)10(12)14-2/h3-5H,6H2,1-2H3

74733-27-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4-(bromomethyl)-2-methoxybenzoate

1.2 Other means of identification

Product number -
Other names METHYL 4-BROMOMETHYL-2-METHOXYBENZOATE

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:74733-27-0 SDS

74733-27-0Downstream Products

74733-27-0Relevant articles and documents

Structure-Guided Design of Novel, Potent, and Selective Macrocyclic Plasma Kallikrein Inhibitors

Li, Zhe,Partridge, James,Silva-Garcia, Abel,Rademacher, Peter,Betz, Andreas,Xu, Qing,Sham, Hing,Hu, Yunjin,Shan, Yuqing,Liu, Bin,Zhang, Ying,Shi, Haijuan,Xu, Qiong,Ma, Xubo,Zhang, Li

, p. 185 - 190 (2017)

A series of macrocyclic analogues were designed and synthesized based on the cocrystal structure of small molecule plasma kallikrein (pKal) inhibitor, 2, with the pKal protease domain. This led to the discovery of a potent macrocyclic pKal inhibitor 29, w

A pharmaceutical composition containing 2-hydroxy-7-methyl octahydrophenanthrene derivative as an estrogen receptor ligand or a pharmaceutically acceptable salt thereof as an effective component

-

, (2017/01/02)

Provided are a compound represented by chemical formulas I and II, or a pharmaceutically acceptable ester, amide, or carbamate salt thereof; and a solvent compound comprising a solvent compound of the ester, amide, or carbamate salt thereof. In addition, provided are use of the compound in treating or preventing diseases or disorders related to activation of an estrogen receptor, and a pharmaceutical composition comprising the compound. In chemical formulas I and II, definitions of R_1, R_2, R_3, and R_4 are the same as those in the specification.COPYRIGHT KIPO 2016

Mild Benzylic Monobromination of Methyl Toluates in Aqueous CTAB

Reddy, Kancharla Rajendar,Rajanna, Kamatala C.,Venkateswarlu, Marri,Saiprakash

, p. 2485 - 2487 (2015/07/27)

A strategy has been developed for the regioselective monobromination of methyl toluates by using tert-butylhydrogen peroxide and potassium bromide (TBHP/KBr) in a cetyltrimethylammonium bromide (CTAB) micellar medium. Ultrasonic and microwave-assisted protocols recorded increased rates and product yields under mild reaction conditions, coupled with a straightforward isolation procedure.

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