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Benzenamine, N-(2-nitro-2-phenylethenyl)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73025-57-7

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73025-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73025-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,2 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73025-57:
(7*7)+(6*3)+(5*0)+(4*2)+(3*5)+(2*5)+(1*7)=107
107 % 10 = 7
So 73025-57-7 is a valid CAS Registry Number.

73025-57-7SDS

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 (Z)-2-Anilino-1-nitro-1-phenylethene

1.2 Other means of identification

Product number -
Other names (Z)-α-Nitro-β-anilinostyrol

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:73025-57-7 SDS

73025-57-7Downstream Products

73025-57-7Relevant academic research and scientific papers

Nucleophilic vinyl substitution in 1-Arylthio(sulfonyl)-2-nitroalkenes

Pavlova,Lipina,Kasem,Kuz'mina

, p. 1321 - 1325 (2007/10/03)

Reactions of 1-arylthio-2-nitroalkenes and 1-arylsulfonyl-2-nitroalkenes with N-, O-, and S-nucleophiles result in replacement of the sulfur-containing group. 1-Arylthio-2-nitroalkenes react with arenethiolates with replacement of the nitro group, yielding the corresponding 1,2-bis(arylthio)alkenes.

S-methyl methaneimidothioates as enamine precursors. A simple procedure for synthesis of 2-nitroenamines

Turner, Kathleen A.

, p. 139 - 141 (2007/10/03)

2-Nitroalken-1-amines are prepared by condensation of substituted nitromethanes with S-methyl methaneimidothioates in the absence of solvent.

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