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104354-36-1

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104354-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104354-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,3,5 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104354-36:
(8*1)+(7*0)+(6*4)+(5*3)+(4*5)+(3*4)+(2*3)+(1*6)=91
91 % 10 = 1
So 104354-36-1 is a valid CAS Registry Number.

104354-36-1SDS

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 (S)-2-amino-1,1-diphenyl-4-(methylthio)-1-butanol

1.2 Other means of identification

Product number -
Other names (S)-2-amino-4-methylsulfanyl-1.1-diphenyl-butanol-(1)

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:104354-36-1 SDS

104354-36-1Relevant articles and documents

Asymmetric reduction of prochiral ketones with N-sulfonylated amino alcohols as catalysts

Zhou, Zhongqiang,Guo, Yajing

, p. 684 - 696 (2008/09/16)

Novel N-sulfonylated amino alcohols were synthesized from L-amino acids and (+)-camphor, and their application to asymmetric reduction of prochiral ketones with NaBH4-BF3·Et2O is described. Copyright Taylor & Francis Group, LLC.

Copper(II) in Organic Synthesis. XI. Evaluation of the Ligand Architecture on the Efficiency of a Copper(II) Catalyst for Enantioselective Michael Reactions.

Desimoni, Giovanni,Dusi, Guglielmo,Faita, Giuseppe,Quadrelli, Paolo,Righetti, PierPaolo

, p. 4131 - 4144 (2007/10/02)

Several bis-copper(II) complexes with chiral ligands derived from 2-substituted 2-(salicylideneamino)ethanols have been tested as catalysts of enantioselective Michael reactions.The degree of enantioselection is strongly affected by the architecture of the ligand.The best result (75percent e.e.) was obtained for a ligand having a substituent potentially suitable to induce the formation of a bis-tetradentate copper(II) complex with a square pyramidal coordination.

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