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95341-86-9

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95341-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95341-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,4 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95341-86:
(7*9)+(6*5)+(5*3)+(4*4)+(3*1)+(2*8)+(1*6)=149
149 % 10 = 9
So 95341-86-9 is a valid CAS Registry Number.

95341-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-(4,5-dihydro-2,5-diphenyloxazol-4-yl)methanol

1.2 Other means of identification

Product number -
Other names ((4S,5S)-2,5-Diphenyl-4,5-dihydro-oxazol-4-yl)-methanol

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:95341-86-9 SDS

95341-86-9Relevant articles and documents

(4S,5S)-(+)-Hydroxymethyl-2,5-diphenyloxazoline

Gzella, Andrzej,Rozwadowska, Maria D.

, p. 981 - 982 (2000)

-

New homochiral bis(oxazoline) ligands for asymmetric catalysis

Hoarau,Ait-Haddou,Castro,Balavoine

, p. 3755 - 3764 (2007/10/03)

Several homochiral bis(oxazolines), with asymmetric centers on the oxazoline rings and on the side chains, were prepared from (1S,2S)-(+)-2-amino-1-phenyl-1,3-propanediol in high yields. Asymmetric cyclopropanation of styrene with ethyl diazoacetate in th

Enantiomerically pure oxazolines tethered to alcohols. Preparation and use in asymmetric catalysis

Allen,Williams

, p. 277 - 282 (2007/10/02)

A series of enantiomerically pure oxazolines tethered to alcohols have been prepared. The use of these oxazolines has been demonstrated in the catalysed addition of diethylzine to aromatic aldehydes to afford the corresponding secondary alcohols with modest levels of asymmetric induction.

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