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95071-02-6

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95071-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95071-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,7 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95071-02:
(7*9)+(6*5)+(5*0)+(4*7)+(3*1)+(2*0)+(1*2)=126
126 % 10 = 6
So 95071-02-6 is a valid CAS Registry Number.

95071-02-6SDS

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 rac-dimethyl (1,3-diphenyl-2-propen-1-yl)malonate

1.2 Other means of identification

Product number -
Other names dimethyl 2-(1,3-diphenylallyl)malonate

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:95071-02-6 SDS

95071-02-6Relevant articles and documents

Chiral Phosphinoferrocenyl-Calixarenes

Karpus, Andrii,Yesypenko, Oleksandr,Boiko, Vyacheslav,Poli, Rinaldo,Daran, Jean-Claude,Voitenko, Zoia,Kalchenko, Vitaly,Manoury, Eric

, p. 3386 - 3394 (2016)

The Mitsunobu alkylation of 4-tert-butylcalix[4]arene with (S)-(2-diphenylthiophosphinoferrocenyl)methanol followed by desulfuration of the thiophosphine unit using tris(dimethylamino)phosphine afforded enantiomerically pure calixarene mono- and di(ferroc

A bidentate resorcinarene-based palladium carbene complex

Ngodwana, Lonwabo,Bose, Sritama,Smith, Vincent J.,Van Otterlo, Willem A. L.,Arnott, Gareth E.

, p. 1923 - 1929 (2017)

The synthesis and characterization of a distally bridged, bidentate resorcinarene bis(carbene) palladium complex is described for the first time. Preliminary catalytic studies show promise for future developments along this framework.

Chiral (E)-2-(1, 3-diaryl allyl) dimethyl malonate compounds and preparation method thereof

-

Paragraph 0003; 0041-0045; 0054-0056, (2021/05/22)

The invention provides chiral (E)-2-(1, 3-diaryl allyl) dimethyl malonate compounds and a preparation method thereof, the method adopts a chiral Pd catalyst to catalyze asymmetric substitution reaction of (E)-1, 3-diaryl allyl acetate compound and dimethy

Chiral P*,S-bidentate diamidophosphites with 1,2-thioether alcohol–based exocyclic substituents in asymmetric Pd-catalyzed reactions

Chuchelkin, I. V.,Firsin, I. D.,Gavrilov, K. N.,Gavrilov, V. K.,Goulioukina, N. S.,Trunina, V. M.,Zheglov, S. V.,Zimarev, V. S.

, (2021/11/01)

Chiral P*,S-diamidophosphites with a 1,3,2-diazaphospholidine core and exocyclic 1,2-hydroxyl-thioether fragments were prepared. These asymmetric inducers provided up to 86% ee in the Pd-catalyzed allylic substitution of (E)-1,3-diphenylallyl acetate with

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