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289039-82-3

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289039-82-3 Usage

General Description

METHYL 5-CHLORO-2-IODOBENZOATE is a chemical compound with the molecular formula C8H6ClIO2. It is a derivative of benzoic acid and belongs to the class of organic compounds known as benzoate esters. METHYL 5-CHLORO-2-IODOBENZOATE is used in various chemical reactions and synthesis processes, particularly in the pharmaceutical and agrochemical industries. It is also used as an intermediate in the production of other organic compounds and has potential applications in materials science and biochemistry. METHYL 5-CHLORO-2-IODOBENZOATE is important for its role in diverse chemical processes and its potential for creating new materials and products.

Check Digit Verification of cas no

The CAS Registry Mumber 289039-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,0,3 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 289039-82:
(8*2)+(7*8)+(6*9)+(5*0)+(4*3)+(3*9)+(2*8)+(1*2)=183
183 % 10 = 3
So 289039-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClIO2/c1-12-8(11)6-4-5(9)2-3-7(6)10/h2-4H,1H3

289039-82-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL 5-CHLORO-2-IODOBENZOATE

1.2 Other means of identification

Product number -
Other names 5-Chloro-2-iodobenzoicacid methyl ester

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:289039-82-3 SDS

289039-82-3Relevant articles and documents

In situ catalytic generation of allylcopper species for asymmetric allylation: Toward 1H-isochromene skeletons

Kawai, Junya,Chikkade, Prasanna Kumara,Shimizu, Yohei,Kanai, Motomu

, p. 7177 - 7180 (2013)

Stay active: Allylcopper species can be generated in situ through catalytic intramolecular oxycupration of allenic alcohol. The allylcopper can react with various aldehydes and a ketone to give 1H-isochromene derivatives in an enantioselective manner (see scheme; HMPA=hexamethylphosphoramide, THF=tetrahydrofuran). The protocol is atom-economical, highly regioselective, stereoconvergent, and tolerant to free hydroxy groups. Copyright

ISOCHROMENE DERIVATIVES AS PHOSHOINOSITIDE 3-KINASES INHIBITORS

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Paragraph 0574; 0575; 0576, (2015/06/24)

Compounds of formula (I) described herein are useful for inhibiting phosphoinositide 3-kinases (PI3K) and the treatment of disorders associated with PI3K enzymes.

BENZO [C] ISOXAZOLOAZEPINE BROMODOMAIN INHIBITORS AND USES THEREOF

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Paragraph 00144; 00151; 00152, (2014/01/08)

The present invention relates to compounds useful as inhibitors of bromodomain- containing proteins. The invention also provides pharmaceutically acceptable compositions comprising compounds of the present invention and methods of using said compositions

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