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1,3,5-Benzenetriol, 2-[3,5-bis(acetyloxy)-4-[3,5-bis(acetyloxy)phenoxy]phenoxy]-, triacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81757-70-2

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81757-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81757-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,5 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81757-70:
(7*8)+(6*1)+(5*7)+(4*5)+(3*7)+(2*7)+(1*0)=152
152 % 10 = 2
So 81757-70-2 is a valid CAS Registry Number.

81757-70-2SDS

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 2,2',4,6,6'-pentaacetoxy-1'-(3,5-diacetoxyphenoxy)biphenyl ether

1.2 Other means of identification

Product number -
Other names triphlorethol-A heptaacetate

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:81757-70-2 SDS

81757-70-2Downstream Products

81757-70-2Relevant academic research and scientific papers

Polyhydroxy Biphenyl Ethers from the Brown Alga Cystophora congesta

Gregson, Richard P.,Daly, John J.

, p. 649 - 657 (2007/10/02)

Two new phloroglucinol polymers have been isolated from the aqueous extract of the brown alga Cystophora congesta.They are the linear trimer 2,2',4,6,6'-pentahydroxy-1'-(3,5-dihydroxyphenoxy)-biphenyl ether (1) and the isomeric angular trimer 3,4',5,6'- or 3,3',5,5'-trtrahydroxy-2'-(3,4,5-trihydroxyphenoxy)biphenyl ether which was characterized as its heptaacetoxy derivative (4).Structures were elucidated principally from an analysis of 13C n.m.r. chemical shifts and 13C-1H spin-spin coupling data.X-ray analysis was performed on the heptaacetoxy derivative of (1) to distinguish it from a regio-isomer(3).

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