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Butanenitrile, 3-methyl-2-[(phenylmethylene)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73405-08-0

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73405-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73405-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,0 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73405-08:
(7*7)+(6*3)+(5*4)+(4*0)+(3*5)+(2*0)+(1*8)=110
110 % 10 = 0
So 73405-08-0 is a valid CAS Registry Number.

73405-08-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzylideneamino)-3-methylbutanenitrile

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:73405-08-0 SDS

73405-08-0Downstream Products

73405-08-0Relevant academic research and scientific papers

Transitioning enantioselective indicator displacement assays for α-amino acids to protocols amenable to high-throughput screening

Leung, Diana,Anslyn, Eric V.

, p. 12328 - 12333 (2008)

Enantioselective indicator displacement assays (eIDAs) for α-amino acids were conducted in a 96-well plate format to demonstrate the viability of the technique for the high-throughput screening (HTS) of enantiomeric excess (ee) values. Chiral receptors [CuII(1)]2+ and [Cu II(2)]2+ with the indicator chrome azurol S were implemented for the eIDAs. Enantiomeric excess calibration curves were made using both receptors and then used to analyze true test samples. These results were compared to those previously obtained with a conventional UV-vis spectrophotometer, and they showed little to no loss of accuracy, while the speed of analysis was increased. A sample of valine of unknown ee was synthesized through an asymmetric reaction to produce a realistic reaction sample, which was analyzed using receptor [CuII(1)]2+. The experimentally determined ee using our eIDA was compared to that obtained by chiral HPLC and 1H NMR chiral shift reagent analysis. This gave errors of 4.7% and 12.0%, respectively. In addition to the use of ee calibration curves, an artificial neural network (ANN) was used to determine the % L-amino acid of the test samples and of the sample of valine of unknown ee from the asymmetric reaction. This method obtained errors of 5.9% and 2.2% compared to chiral HPLC and 1H NMR chiral shift reagent analysis, respectively. The technique using calibration curves for the determination of ee on a 96-well plate allows one to determine 96 ee values in under a minute, enabling its use for HTS of asymmetric reactions with acceptable accuracy.

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