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137472-16-3

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137472-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137472-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,7 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 137472-16:
(8*1)+(7*3)+(6*7)+(5*4)+(4*7)+(3*2)+(2*1)+(1*6)=133
133 % 10 = 3
So 137472-16-3 is a valid CAS Registry Number.

137472-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [3,5-bis[[3,5-bis[[3,5-bis(phenylmethoxy)phenyl]methoxy]phenyl]methoxy]phenyl]methyl alcohol

1.2 Other means of identification

Product number -
Other names {3,5-Bis-[3,5-bis-(3,5-bis-benzyloxy-benzyloxy)-benzyloxy]-phenyl}-methanol

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:137472-16-3 SDS

137472-16-3Relevant articles and documents

A fast double-stage convergent synthesis of dendritic polyethers

L'abbe, Gerrit,Forier, Bart,Dehaen, Wim

, p. 2143 - 2144 (1996)

Two tert-butyldiphenylsilyl-protected synthons 7 and 9 are prepared in excellent yields and used in a one-pot synthesis of higher generation polyether dendrons.

Optical switching and antenna effect of dendrimers with an anthracene core

Cao, Derong,Dobis, Silvia,Gao, Chunmei,Hillmann, Sabine,Meier, Herbert

, p. 9317 - 9323 (2008/12/20)

Dendrimers 6Gi (i=1-4) consisting of an anthracene core and Frechet dendrons which are attached via a CH2OCH2 chain in the 9-position undergo quantitative and completely reversible intramolecular [4π+4π] cycloaddition. The

Photoisomerization of stilbene dendrimers: The need for a volume-conserving isomerization mechanism

Uda, Mayuko,Mizutani, Takuo,Hayakawa, Junpei,Momotake, Atsuya,Ikegami, Masashi,Nagahata, Ritsuko,Arai, Tatsuo

, p. 596 - 605 (2007/10/03)

Highly branched stilbene dendrimers were synthesized and their photochemical behavior was studied. Even the stilbene dendrimer with molecular weight over 6500 underwent transcis isomerization in the excited singlet state within the lifetime of 10 ns. The

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