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N-(2,4-dinitrophenyl)-2,4-dinitroaniline is a chemical compound with the molecular formula C12H6N6O7. It is an organic compound that features two nitro groups (-NO2) attached to both the aniline (C6H5NH2) and phenyl (C6H5) parts of the molecule. N-(2,4-dinitrophenyl)-2,4-dinitroaniline is known for its yellow crystalline appearance and is often used in the synthesis of dyes and pigments due to its intense color. It is also a component in some chemical research studies, particularly those involving the exploration of nitroaromatic compounds and their properties. The compound's structure and properties make it a subject of interest in the field of organic chemistry, where it can be used to understand the behavior of molecules with multiple nitro groups.

2908-76-1

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2908-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2908-76-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2908-76:
(6*2)+(5*9)+(4*0)+(3*8)+(2*7)+(1*6)=101
101 % 10 = 1
So 2908-76-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H7N5O8/c18-14(19)7-1-3-9(11(5-7)16(22)23)13-10-4-2-8(15(20)21)6-12(10)17(24)25/h1-6,13H

2908-76-1SDS

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 N-(2,4-dinitrophenyl)-2,4-dinitroaniline

1.2 Other means of identification

Product number -
Other names Benzenamine, N-(2,4-dinitrophenyl)-2,4-dinitro-

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:2908-76-1 SDS

2908-76-1Downstream Products

2908-76-1Relevant academic research and scientific papers

Pd(OAc)2-catalyzed dinitration reaction of aromatic amines

Feng, Yi-Si,Mao, Long,Bu, Xiao-Song,Dai, Jian-Jun,Xu, Hua-Jian

, p. 3827 - 3832 (2015/06/02)

Taking advantage of Pd(OAc)2-catalyzed dinitration reactions with Bi(NO3)3·5H2O in trifluoroethanol (TFE) and trifluoroacetic acid (TFA), we have developed an efficient and practical method for the synthesis of secondary dinitro-aromatic amines. The products could be applied to the preparation of 5-amine-N-methyl-benzimidazolone, the azo-dyes, economic advantages. The method has also been expanded to the dinitration reaction of some tertiary aromatic amines.

A novel N-N bond cleavage in 1,5-diaminotetrazole: Synthesis and characterization of 5-picrylamino-1,2,3,4-tetrazole (PAT)

Tang, Yongxing,Yang, Hongwei,Ju, Xuehai,Huang, Hui,Lu, Chunxu,Cheng, Guangbin

, p. 4127 - 4131 (2014/03/21)

The reaction of 1,5-diaminotetrazole with picryl chloride (PiCl) forms 5-picrylamino-1,2,3,4-tetrazole (PAT) rather than the expected 1-picrylamino-5-amino-1,2,3,4-tetrazole or 5-picrylamino-1-amino-1,2,3,4- tetrazole. The structure of PAT was confirmed by single-crystal X-ray diffraction. Some of the energetic properties of the synthesized compound were also studied.

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