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87974-55-8

87974-55-8

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87974-55-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87974-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,7 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87974-55:
(7*8)+(6*7)+(5*9)+(4*7)+(3*4)+(2*5)+(1*5)=198
198 % 10 = 8
So 87974-55-8 is a valid CAS Registry Number.

87974-55-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[1-(3-nitrophenyl)ethylidene]hydroxylamine

1.2 Other means of identification

Product number -
Other names 3-nitroacetophenone oxime

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:87974-55-8 SDS

87974-55-8Upstream product

87974-55-8Relevant articles and documents

One-pot synthesis of 2-amino-3,4-dicyanopyridines from ketoximes and tetracyanoethylene via Cu(I)-catalyzed cyclization

Han, Ziwei,Lv, Jianguang,Zhang, Jianmin

supporting information, p. 2162 - 2168 (2019/02/25)

A novel approach to 2-amino-3,4-dicyanopyridines has been discovered from Cu(I)-catalyzed cyclizations of simple and easily available ketoximes and tetracyanoethylene (TCNE). The complexed radical mechanism involves cleavage of several O[sbnd]H/N[sbnd]O/C

Gas-phase acidities of acetophenone oximes. Substituent effect and solvent effects

Badal, Mizanur Rahman,Mishima, Masaaki

experimental part, p. 58 - 65 (2010/03/25)

Gas-phase acidities (GA) of ring-substituted (E)-acetophenone oximes, XC6H4C(CH3)=NOH, were determined by measuring proton-transfer equilibria using an FT-ICR mass spectrometer. The magnitude of the substituent effect on t

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