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Bicyclo[2.2.1]heptan-2-ol, 7-(ethylmethylamino)-, (1R,2R,4R,7S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

774577-04-7

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  • Bicyclo[2.2.1]heptan-2-ol, 7-(ethylmethylamino)-, (1R,2R,4R,7S)- (9CI)

    Cas No: 774577-04-7

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774577-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 774577-04-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,4,5,7 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 774577-04:
(8*7)+(7*7)+(6*4)+(5*5)+(4*7)+(3*7)+(2*0)+(1*4)=207
207 % 10 = 7
So 774577-04-7 is a valid CAS Registry Number.

774577-04-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Bicyclo[2.2.1]heptan-2-ol, 7-(ethylmethylamino)-, (1R,2R,4R,7S)- (9CI)

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

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More Details:774577-04-7 SDS

774577-04-7Downstream Products

774577-04-7Relevant articles and documents

An efficient synthesis of enantiopure (+)- and (-)-syn-1,3-amino alcohols with a norbornane framework and their application in the asymmetric addition of ZnEt2 to benzaldehyde

De Oliveira, Luciane F.,Costa, Valentim E.U.

, p. 2583 - 2590 (2004)

A series of new optically active (+)- and (-)-syn-1,3-amino alcohols with a norbornane framework has been synthesized. Their abilities as chiral catalysts in the enantioselective additions of ZnEt2 to benzaldehyde were evaluated. High yields and enantiomeric excesses have been achieved (up to 91%). The influence of the configuration of the carbon bearing the hydroxyl group of the ligands has been studied. A plausible mechanism is also suggested for the observed enantioselectivity.

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