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82212-55-3

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82212-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82212-55-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,1 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82212-55:
(7*8)+(6*2)+(5*2)+(4*1)+(3*2)+(2*5)+(1*5)=103
103 % 10 = 3
So 82212-55-3 is a valid CAS Registry Number.

82212-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-2-(fluoromethyl)-5-phenylmethoxypentanenitrile

1.2 Other means of identification

Product number -
Other names 2-fluoromethyl-2-amino-5-benzyloxypentanenitrile

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:82212-55-3 SDS

82212-55-3Relevant articles and documents

2-(4-Amino-4-carboxybutyl)aziridine-2-carboxylic acid. A potent irreversible inhibitor of diaminopimelic acid epimerase. Spontaneous formation from α-(halomethyl)diaminopimelic acids

Gerhart,Higgins,Tardif,Ducep

, p. 2157 - 2162 (1990)

2-(4-Amino-4-carboxybutyl)aziridine-2-carboxylic acid (3) (aziridino-DAP) was identified as the product of spontaneous hydrolysis of α-(halomethyl)diaminopimelic acids (α-halomethyl-DAPs) 2a-c. Under physiological conditions, 3 is an extremely potent irre

Process for preparing fluorinated amino-nitriles

-

, (2008/06/13)

Certain α-(fluoromethyl or difluoromethyl)-α-aminoacetonitriles are prepared by treating the appropriate α-(fluoromethyl or difluoromethyl) ketimine magnesium halide with hydrogen cyanide or with an alkali metal cyanide or ammonium cyanide and a proton source. The products are useful as intermediates for making α-(fluoromethyl or difluoromethyl)-α-amino acids having pharmacological activity.

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