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101986-32-7

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101986-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101986-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,9,8 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101986-32:
(8*1)+(7*0)+(6*1)+(5*9)+(4*8)+(3*6)+(2*3)+(1*2)=117
117 % 10 = 7
So 101986-32-7 is a valid CAS Registry Number.

101986-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ((3S,4R)-4-Phenyl-oxazolidin-3-yl)-acetonitrile

1.2 Other means of identification

Product number -
Other names -

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:101986-32-7 SDS

101986-32-7Downstream Products

101986-32-7Relevant articles and documents

Synthesis of morpholin-2-ones by chemoselective intramolecular rhodium-catalyzed reductive ring expansion of oxazolidines

Vasylyev, Maksym,Alper, Howard

supporting information; experimental part, p. 1357 - 1359 (2009/05/07)

(Chemical Equation Presented) The rhodium-catalyzed reductive intramolecular ring expansion of N-(ethoxycarboxymethyl)oxazolidines was carried out under an atmosphere of carbon monoxide and hydrogen to afford N-methylmorpholin-2-ones in good to excellent

aSYMMETRIC SYNTHESIS IV1. PRAPARATION OF CHIRAL α-AMINONITRILES FROM A NEW N-CYANOMETHYL-1,3-OXAZOLIDINE SYNTHON

Marco, Jose L.,Royer, Jagues,Husson, Henri-Philippe

, p. 3567 - 3570 (2007/10/02)

The synthesis of (-)-N-cyanomethyl-4-phenyl-1,3-oxazolidine 1 is reported.Good yields and moderate diastereomeric excesses (d.e.s.) of mono- and di-substituted α-aminonitriles were obtained from simple chiral template.

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