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2,3-Butanediamine, 1,1,4,4-tetranitro-N,N'-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96184-05-3

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96184-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96184-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,8 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96184-05:
(7*9)+(6*6)+(5*1)+(4*8)+(3*4)+(2*0)+(1*5)=153
153 % 10 = 3
So 96184-05-3 is a valid CAS Registry Number.

96184-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,4,4-tetranitro-2-N,3-N-diphenylbutane-2,3-diamine

1.2 Other means of identification

Product number -
Other names 2,3-di(phenylamino)-1,1,4,4-tetranitrobutane

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:96184-05-3 SDS

96184-05-3Downstream Products

96184-05-3Relevant academic research and scientific papers

1,1,4,4-TETRANITRO-1,3-BUTADIENE - AN INTERMEDIADE IN THE CHEMICAL TRANSFORMATION OF THE DIACETATE OF 1,1,4,4-TETRANITRO-2,3-BUTANEDIOL

Nekrasova, G. V.,Lipina, E. S.,Pozdnyakov, V. P.,Perekalin, V. V.

, p. 2277 - 2281 (2007/10/02)

The behavior of the diacetate of 1,1,4,4-tetranitro-2,3-butanediol in various media was studied in order to investigate the possibility of the synthesis of 1,1,4,4-tetranitro-1,3-butadiene.It was established that deacetylation takes place readily under normal conditions in the presence of bases (OH- and OCH3- ions, aniline), with which the tetranitrobutadiene produced in situ forms bisaddition products.The production of tetranitrobutadiene as intermediate is also confirmed by the fact that charge-transfer complexes, which are in time transformed into the products from the reaction with the base, are formed in the presence of donors.

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