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Butanenitrile, 2-diazo-3-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65950-83-6

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65950-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65950-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,5 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65950-83:
(7*6)+(6*5)+(5*9)+(4*5)+(3*0)+(2*8)+(1*3)=156
156 % 10 = 6
So 65950-83-6 is a valid CAS Registry Number.

65950-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyano-1-diazonioprop-1-en-2-olate

1.2 Other means of identification

Product number -
Other names Butanenitrile,2-diazo-3-oxo

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:65950-83-6 SDS

65950-83-6Downstream Products

65950-83-6Relevant academic research and scientific papers

Synthesis and Spectral Characterization of Azidoketenimines

L'abbe, Gerrit,Godts, Francoise

, p. 748 - 750 (1983)

The first azidoketenimines (6a,b) have been generated from the 3-unsubstituted 4-azidoisoxazoles (3a,b) by successive quaternization and treatment with triethylamine at -90 deg C.

SYNTHESIS AND THERMAL DECOMPOSITION OF 4-AZIDOISOXAZOLES

L'abbe, Gerrit,Godts, Francoise

, p. 229 - 236 (2007/10/02)

The diazonium salts derived from 1a,b decompose at 0 deg C to give α-cyanodiazoketones 3a,b and, in the case of 1b, also the N-hydroxytriazole 4.The azides 2a,b were prepared from the diazonium salts at -15 deg C.The diazonium salt from 1c is more stable and can be converted into the azide 2c at 0 deg C, along with formation of 5 as a side product.Kinetic measurements have been carried out for the thermal fragmentation of 2a - c which indicated that the reactions occur by a concerted mechanism.

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