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138771-02-5

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138771-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138771-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,7 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 138771-02:
(8*1)+(7*3)+(6*8)+(5*7)+(4*7)+(3*1)+(2*0)+(1*2)=145
145 % 10 = 5
So 138771-02-5 is a valid CAS Registry Number.

138771-02-5SDS

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 1,2-bis(3-formyl-4-phenyl)ethane

1.2 Other means of identification

Product number -
Other names 2,2'-diformyldiphenylethane

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:138771-02-5 SDS

138771-02-5Relevant articles and documents

Exo-functionalized shape-persistent [2+3] cage compounds: Influence of molecular rigidity on formation and permanent porosity

Schneider, Markus W.,Oppel, Iris M.,Mastalerz, Michael

supporting information; experimental part, p. 4156 - 4160 (2012/06/01)

Exo-functionalized [2+3] cage compounds were synthesized by using two different bissalicylaldehydes as molecular precursors in the reaction with triptycene triamine to study the influence of the rigidity of the molecular structure of [2+3] cages on their

Mechanistic Studies on the Photogenerated Dienol with α-Phenyl-N-tert-Butylnitrones

Pan, Kai,Ho, Tong-Ing

, p. 243 - 247 (2007/10/03)

The mechanism for the photochemical reactions of o-methyl-benzaldehyde (1), o-methyl-acetophenone (2) and o-methyl-benzophenone (3) in the presence of α-phenyl-N-tert-butylnitrone (PBN) to the formation of stable nitroxyl radicals 4-6 is studied. The nitroxyl radical product 6 can also be obtained by the thermolysis of benzocyclobutenol with PBN. Thus, the radical products were derived from a novel and regioselective 4+2 cycloaddition of the photogenerated dienol intermediate with PBN.

Synthesis of Polynuclear Aromatic Dialdehyde in HF-SbF5

Tanaka, Mutsuo,Fujiwara, Masahiro,Ando, Hisanori,Souma, Yoshie

, p. 3213 - 3215 (2007/10/02)

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