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61149-80-2

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61149-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61149-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,4 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61149-80:
(7*6)+(6*1)+(5*1)+(4*4)+(3*9)+(2*8)+(1*0)=112
112 % 10 = 2
So 61149-80-2 is a valid CAS Registry Number.

61149-80-2SDS

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 N-methyl-3,4-dinitroaniline

1.2 Other means of identification

Product number -
Other names N-Methyl-3,4-dinitro-anilin

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:61149-80-2 SDS

61149-80-2Downstream Products

61149-80-2Relevant articles and documents

Synthesis, properties, and molecular structure of nitro-substituted N-methyl-N-nitroanilines

Prezhdo,Bykova,Prezhdo,Daszkiewicz,Kyziol,Zaleski

, p. 64 - 75 (2007/10/03)

Ten mono-, di-, and trinitro derivatives of N-methyl-N-nitroaniline were synthesized and studied by spectral, electrooptical, and quantum-chemical methods. Three of these derivatives, N-methyl-N,2,3-trinitroaniline, N-methyl-N,2,5-trinitroaniline, N-methyl-N,3,5-trinitroaniline, were also examined by the X-ray diffraction method. The N-nitroamino group in their molecules is almost planar, the N7-N8 bond is shortened, and the N8 atom is characterized by a strong deficit of electron density. The dihedral angle between the planes of the N-nitroamino group and the benzene ring is 56°-92°, which makes conjugation between these fragments impossible. The N-nitroamino group in the examined compounds acts as a weak electron donor with respect to the nitro groups in the aromatic ring; the mechanism of this effect is inductive. Pleiades Publishing, Inc. 2006.

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