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212688-02-3

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212688-02-3 Usage

General Description

Methyl-3,5-dibromo-4-hydroxyphenylacetate is a chemical compound that belongs to the class of phenylacetates. It is a methyl ester derivative of 3,5-dibromo-4-hydroxyphenylacetic acid, which is a brominated derivative of phenylacetic acid. METHYL-3,5-DIBROMO-4-HYDROXYPHENYLACETATE is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential antimicrobial and antioxidant properties. Overall, methyl-3,5-dibromo-4-hydroxyphenylacetate has a range of potential applications in various industries due to its unique chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 212688-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,6,8 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 212688-02:
(8*2)+(7*1)+(6*2)+(5*6)+(4*8)+(3*8)+(2*0)+(1*2)=123
123 % 10 = 3
So 212688-02-3 is a valid CAS Registry Number.

212688-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,5-dibromo-4-hydroxyphenyl)propanoate

1.2 Other means of identification

Product number -
Other names METHYL-3,5-DIBROMO-4-HYDROXYPHENYLACETATE

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:212688-02-3 SDS

212688-02-3Relevant articles and documents

Synthesis of (+)-O-methylthalibrine by employing a stereocontrolled Bischler-Napieralski reaction and an electrochemically generated diaryl ether

Kawabata, Yuki,Naito, Yu,Saitoh, Tsuyoshi,Kawa, Kohei,Fuchigami, Toshio,Nishiyama, Shigeru

, p. 99 - 104 (2014/01/06)

An efficient electrochemical four-step route was developed for the preparation of diaryl ether derivatives by using halogenation and dehalogenation processes in addition to electrochemical phenolic oxidation and reduction reactions. The synthesis of (+)-O

Total synthesis of antibacterial dibromotyrosine derived alkaloid purpuramine-K#

Reddy, S. Malla,Srinivasulu,Venkateswarlu

, p. 2757 - 2762 (2007/10/03)

The first total synthesis of a dibromotyrosine derived alkaloid purpuramine K 1 reported for possible anti-bacterial activity against gram-positive bacteria viz: Staphylococcus aureus, Bacillus subtilis, Bacillus sphaericus and gram-negative bacteria like Chromobacterium violaceum, Klebsiella aerogenes, and Pseudomonas aeruginosa has been achieved. The synthesis involves preparation of methyl-3-bromopropyl carbamate 6, and Boc protected 2-[3,5-dibromo, 4-hydroxy phenyl] ethyl amine 13 which is followed by coupling of these two structural fragments to give corresponding ether 14. After deprotection of Boc group in compound 14, it is reacted with 4-hydroxyphenyl pyruvic acid oxime derivative 17 using EDCI/HOBT to give compound 18, which is further transformed to purpuramine K.

Thyroid receptor ligands and method

-

, (2008/06/13)

Novel thyroid receptor ligands are provided which have the general formula (I) where R1is alkyl of 1 to 4 carbons or cycloalkyl of 3 to 7 carbons; R2and R3are the same or different and are hydrogen, halogen, alkyl of 1 to

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