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85784-34-5

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85784-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85784-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,8 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85784-34:
(7*8)+(6*5)+(5*7)+(4*8)+(3*4)+(2*3)+(1*4)=175
175 % 10 = 5
So 85784-34-5 is a valid CAS Registry Number.

85784-34-5SDS

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 methyl 2-[3-(2-methoxy-2-oxoethoxy)phenoxy]acetate

1.2 Other means of identification

Product number -
Other names methyl 2-<3-<(methoxycarbonyl)methoxy>phenoxy> acetate

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:85784-34-5 SDS

85784-34-5Relevant articles and documents

A Family of Metal-Organic Frameworks with a New Chair-Conformation Resorcin[4]arene-Based Ligand: Selective Luminescent Sensing of Amine and Aldehyde Vapors, and Solvent-Mediated Structural Transformations

Zhang, Hang,Yang, Jin,Liu, Ying-Ying,Song, Shuyan,Ma, Jian-Fang

, p. 3244 - 3255 (2016)

By utilizing a new chair-conformation resorcin[4]arene-based octacarboxylate ligand, four functional metal-organic frameworks (MOFs), namely, [(CH3)2NH2]4[Cd2(L)]·4H2O (1), [(CH3

Novel synthesis of resorcinarene O-acetates by BF3·OEt2-catalyzed cyclocondensation of 1,3-(dialkoxycarbonylmethoxy)benzenes with aldehydes

Zhou, Rui,Ren, Jia Chao,Yan, Chao Guo

body text, p. 335 - 342 (2011/11/29)

Resorcinarene O-acetates, which are key intermediates in the chemical modification process of resorcinarene, can be efficiently prepared in high yields by BF3·OEt2 catalyzed cyclocondensation of 1,3-(dialkoxycarbonylmethoxy)benzenes

Synthesis and antiviral activity of new bisacridinylhydrazides of aryloxyacetic acids

Lyakhov,Lyakhova,Panchenko,Litvinova,Andronati

, p. 653 - 656 (2007/10/03)

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