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158361-26-3

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158361-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158361-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,3,6 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 158361-26:
(8*1)+(7*5)+(6*8)+(5*3)+(4*6)+(3*1)+(2*2)+(1*6)=143
143 % 10 = 3
So 158361-26-3 is a valid CAS Registry Number.

158361-26-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N′-ditosyl-meso-cyclopent-4-ene-1,3-diol biscarbamate

1.2 Other means of identification

Product number -
Other names meso-cyclopent-2-ene-1,4-diol

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:158361-26-3 SDS

158361-26-3Relevant articles and documents

Palladium catalyzed asymmetric reactions assisted by P*,P*-bidentate bisdiamidophosphites based on 1,4-diols

Gavrilov, Konstantin N.,Zheglov, Sergey V.,Gavrilov, Vladislav K.,Maksimova, Marina G.,Tafeenko, Viktor A.,Chernyshev, Vladimir V.,Birin, Kirill P.,Mikhel, Igor S.

, p. 461 - 471 (2017/01/13)

A small series of P*,P*-bidentate bisdiamidophosphite ligands containing 1,3,2-diazaphospholidine rings have been prepared. The cationic [Pd(allyl)(P*,P*)]BF4and neutral [Pd(P*,P*)Cl2] palladium(II) complexes were synthesized with on

Diamidophosphites with remote P*-stereocentres and their performance in Pd-catalyzed enantioselective reactions

Gavrilov, Konstantin N.,Zheglov, Sergey V.,Gavrilov, Vladislav K.,Chuchelkin, Ilya V.,Novikov, Ivan M.,Shiryaev, Alexei A.,Volov, Alexandr N.,Zamilatskov, Ilya A.

, p. 1116 - 1121 (2014/09/17)

Diamidophosphite ligands based on 1,1′-bis(hydroxymethyl)ferrocene or N1,N2-bis((S)-1-hydroxy-3,3-dimethylbutan-2-yl)oxalamide and bearing 1,3,2-diazaphospholidine rings with stereogenic phosphorus atoms were obtained. The use of the

Phosphites and diamidophosphites based on mono-ethers of BINOL: A comparison of enantioselectivity in asymmetric catalytic reactions

Gavrilov, Konstantin N.,Zheglov, Sergey V.,Gavrilova, Mariya N.,Novikov, Ivan M.,Maksimova, Marina G.,Groshkin, Nikolay N.,Rastorguev, Eugenie A.,Davankov, Vadim A.

scheme or table, p. 1581 - 1589 (2012/03/08)

Novel P-monodentate phosphite-type ligands have been synthesized in one step from BINOL mono-tosylate and BINOL mono-(-)-menthylcarbonate. The use of these ligands provides up to 96% ee in Pd-catalyzed asymmetric allylic substitution of (E)-1,3-diphenylal

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