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3-Oxa-6-azatricyclo[3.2.1.02,4]octan-7-one,(1S,2R,4S,5R)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

329910-40-9

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329910-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 329910-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,9,1 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 329910-40:
(8*3)+(7*2)+(6*9)+(5*9)+(4*1)+(3*0)+(2*4)+(1*0)=149
149 % 10 = 9
So 329910-40-9 is a valid CAS Registry Number.

329910-40-9SDS

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 (1S,2R,4S,5R)-3-Oxa-6-azatricyclo[3.2.1.0<sup>2,4</sup>]octan-7-one

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:329910-40-9 SDS

329910-40-9Relevant academic research and scientific papers

COMPOUNDS AND COMPOSITIONS USEFUL FOR TREATING DISORDERS RELATED TO NTRK

-

Page/Page column 77, (2017/03/14)

This invention relates to inhibitors of NTRK that are active against wild-type NTRK and its resistant mutants.

Highly selective directed hydrogenation of enantiopure 4-(tert-butoxycarbonylamino)cyclopent-1-enecarboxylic acid methyl esters

Smith, Mark E.B.,Derrien, Nadine,Lloyd, Michael C.,Taylor, Stephen J.C.,Chaplin, David A.,McCague, Raymond

, p. 1347 - 1350 (2007/10/03)

The use of both N-tert-butoxycarbonylamino- and hydroxyl-directed hydrogenation methodology to yield essentially single diastereomers of 3-(tert-butoxycarbonylamino)-4-hydroxycyclopentanecarboxylic acid methyl esters and 3-(tert-butoxycarbonylamino)cyclopentanecarboxylic acid methyl esters is described. These results incorporate the first reported carbamate-directed hydrogenations of functionalised cyclopentenes.

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