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8-Azabicyclo[3.2.1]octane-3-carboxylic acid, 3-amino-8-methyl-, exo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75646-79-6

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75646-79-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75646-79-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,4 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75646-79:
(7*7)+(6*5)+(5*6)+(4*4)+(3*6)+(2*7)+(1*9)=166
166 % 10 = 6
So 75646-79-6 is a valid CAS Registry Number.

75646-79-6SDS

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 3β-amino-1αH,5αH-tropane-3α-carboxylic acid

1.2 Other means of identification

Product number -
Other names (1R,3S,5S)-3-Amino-8-methyl-8-aza-bicyclo[3.2.1]octane-3-carboxylic acid

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:75646-79-6 SDS

75646-79-6Downstream Products

75646-79-6Relevant academic research and scientific papers

3-Aminotropane-3-carboxylic acids. Preparation and properties

Trigo, Gregorio G.,Avendano, Carmen,Santos, Emilia,Christensen, Halvor N.,Handlogten, Mary E.

, p. 2295 - 2300 (2007/10/02)

The two isomers of 3-aminotropane-3-carboxylic acid have been prepared by hydrolysis of the two α- and β-tropane-3-spiro-5'-hydantoins whose configurations were determined by X-ray crystallography and 13C nmr.The pK'a values of these amino acids and the hydrolysis rates of their N-formyl derivatives have been determined to study the influence of the amino group in an axial or equatorial position.The biological transport - inhibitory action of the two tropane amino acids has also been compared.

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