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62290-17-9

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62290-17-9 Usage

General Description

Ethyl 3-(bromomethyl)benzoate is a chemical compound that consists of a benzene ring with a bromomethyl group attached to the third carbon atom and an ester group attached to the carbon atom. It is commonly used as a reagent in organic synthesis to introduce the bromomethyl group into various organic molecules. Ethyl 3-(bromomethyl)benzoate is also known for its use in the production of pharmaceuticals and agrochemicals. It is important to handle this chemical with caution as it is flammable and can cause skin and eye irritation upon contact. Furthermore, it should be stored in a cool, dry place and away from sources of heat and ignition.

Check Digit Verification of cas no

The CAS Registry Mumber 62290-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,9 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62290-17:
(7*6)+(6*2)+(5*2)+(4*9)+(3*0)+(2*1)+(1*7)=109
109 % 10 = 9
So 62290-17-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H11BrO2/c1-2-13-10(12)9-5-3-4-8(6-9)7-11/h3-6H,2,7H2,1H3

62290-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-(bromomethyl)benzoate

1.2 Other means of identification

Product number -
Other names 3-(ethoxycarbonyl)benzyl bromide

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:62290-17-9 SDS

62290-17-9Relevant articles and documents

A 4 + 4 strategy for synthesis of zeolitic metal-organic frameworks: An indium-MOF with SOD topology as a light-harvesting antenna

Sun, Libo,Xing, Hongzhu,Liang, Zhiqiang,Yu, Jihong,Xu, Ruren

, p. 11155 - 11157 (2013/11/19)

A zeolitic metal-organic framework with a SOD topology, (Et 2NH2)[In(BCBAIP)]·4DEF·4EtOH (H 4BCBAIP: 5-(bis(4-carboxybenzyl)amino)isophthalic acid) (1), has been constructed by a 4 + 4 synthetic strategy from tetrahedral organic building units and In3+ ions. Compound 1 could adsorb organic dyes and be used as a light-harvesting antenna.

Vitamin d analogues

-

, (2008/06/13)

Compounds of the formula I wherein X represents hydrogen or hydroxy; R1 and R2, which may be the same or different, represent hydrogen, (C1-C4)alkyl optionally substituted with one hydroxyl group or one or more fluorine atoms, or, together with the carbon atom to which they are attached, R1 and R2 form a (C3-C5)carbocyclic ring; R3 represents (C1-C4)alkyl, (C1-C4)alkoxy or a halogen atom, such as fluorine, chlorine, bromine, or iodine, and in-vivo hydrolyzable esters thereof with pharmaceutically acceptable acids, may be used in the prophylaxis and/or treatment of dieases characterized by abnormal cell differentiation and/or cell proliferation.

Synthesis and structure-activity relationships of stilbene retinoid analogs substituted with heteroaromatic carboxylic acids

Beard,Chandraratna,Colon,Gillett,Henry,Marler,Song,Denys,Garst,Arefieg,Klein,Gil,Wheeler,Kochhar,Davies

, p. 2820 - 2829 (2007/10/02)

Retinoids elicit biological responses by activating a series of nuclear receptors. Six retinoid receptors belonging to two families are currently known: retinoic acid receptors (RAR(α,β,andγ)) and retinoid X receptors (RXR(α,β,andγ)). Stilbene retinoid an

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