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Benzene, 1-[2-[3,5-bis(phenylmethoxy)phenyl]ethenyl]-3,5-dibromo-2-(phenylmeth oxy)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88812-24-2

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88812-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88812-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,8,1 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88812-24:
(7*8)+(6*8)+(5*8)+(4*1)+(3*2)+(2*2)+(1*4)=162
162 % 10 = 2
So 88812-24-2 is a valid CAS Registry Number.

88812-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (((5-(2-(benzyloxy)-3,5-dibromostyryl)-1,3-phenylene)bis(oxy))bis(methylene))dibenzene

1.2 Other means of identification

Product number -
Other names -

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:88812-24-2 SDS

88812-24-2Relevant academic research and scientific papers

Liquid Chromatography on Triacetylcellulose, 6. Synthesis, Chromatographic Enrichment of Enantiomers, and Barriers to Enantiomerization of Helical Phenanthrenes

Scheruebl, Herbert,Fritzsche, Ursula,Mannschreck, Albrecht

, p. 336 - 343 (2007/10/02)

Enantiomerization barriers (Table 1) for novel 4,5-disubstituted phenanthrenes of types A and B have been determined by coalescence of 1H NMR signals or by thermal racemization of chromatographically enriched enantiomers.The barriers depend upon the size of the groups R = CMe3, Br, Me, Cl, OBz, in A and B, the behaviour of annelated benzo rings instead of R being particularly considered.

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