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928789-96-2

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928789-96-2 Usage

Uses

Used in the synthesis of chiral 1,2-diarylsubstituted aziridines.

Check Digit Verification of cas no

The CAS Registry Mumber 928789-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,7,8 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 928789-96:
(8*9)+(7*2)+(6*8)+(5*7)+(4*8)+(3*9)+(2*9)+(1*6)=252
252 % 10 = 2
So 928789-96-2 is a valid CAS Registry Number.

928789-96-2 Well-known Company Product Price

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  • Aldrich

  • (693626)  S-N-(3,5-Di-tert-butylphenyl)-3-methyl-2-(N-formyl-N-methylamino)butanamide  96%

  • 928789-96-2

  • 693626-50MG

  • 1,547.91CNY

  • Detail
  • Aldrich

  • (693626)  S-N-(3,5-Di-tert-butylphenyl)-3-methyl-2-(N-formyl-N-methylamino)butanamide  96%

  • 928789-96-2

  • 693626-100MG

  • 2,558.79CNY

  • Detail

928789-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-N-(3,5-ditert-butylphenyl)-2-[formyl(methyl)amino]-3-methylbutanamide

1.2 Other means of identification

Product number -
Other names Sigamide

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:928789-96-2 SDS

928789-96-2Downstream Products

928789-96-2Relevant articles and documents

Enantioselective synthesis of 1,2-diarylaziridines by the organocatalytic reductive amination of α-chloroketones

Malkov, Andrei V.,Stoncius, Sigitas,Kocovsky, Pavel

, p. 3722 - 3724 (2008/02/13)

(Chemical Equation Presented) One-sided triangles: A simple protocol has been developed for the synthesis of highly useful single enantiomers of 1,2-diarylaziridines. The method involves conversion of the readily available α-chloroacetophenones into the c

Organocatalysis with a fluorous tag: Asymmetric reduction of imines with trichlorosilane catalyzed by amino acid-derived formamides

Malkov, Andrei V.,Figlus, Marek,Stoncius, Sigitas,Kocovsky, Pavel

, p. 1315 - 1325 (2007/10/03)

(Chemical Equation Presented) Asymmetric reduction of ketimines 1 with trichlorosilane can be catalyzed by N-methylvaline-derived Lewis-basic formamides 3a-d with high enantioselectivity (≤95% ee) and low catalyst loading (1-5 mol %) at room temperature i

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