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2-Azaspiro[4.5]decane-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93960-17-9

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93960-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93960-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,6 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93960-17:
(7*9)+(6*3)+(5*9)+(4*6)+(3*0)+(2*1)+(1*7)=159
159 % 10 = 9
So 93960-17-9 is a valid CAS Registry Number.

93960-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-azaspiro[4.5]decane-3-carbonitrile

1.2 Other means of identification

Product number -
Other names Spiro[4.5]-2-aza-decane-3-carbonitrile

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:93960-17-9 SDS

93960-17-9Relevant academic research and scientific papers

Spiro-2-aza-alkane-3-carbonitriles, their preparation and their use

-

, (2008/06/13)

The invention provides compounds of the formula I STR1 in which m is 1 to 3 and n is 1 to 4, a process for their preparation, and their use as intermediates for the manufacture of valuable medicaments, and starting products for the preparation of compound

SYNTHESYS OF UNNATURAL AMINO ACIDS: SPIRO-2-AZA-DECAN-CARBOXYLIC ACID

Teetz, V.,Gaul, H.

, p. 4483 - 4486 (2007/10/02)

Spiro-2-aza-alkan-carboxylic acids represent bulky proline analogues with increased lipophilicity.They are readily available from cyclic nitriles via alkylation with bromoacetaldehyde acetals, reduction to the corresponding amine, cyclisation to the

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