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7403-39-6

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7403-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7403-39-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7403-39:
(6*7)+(5*4)+(4*0)+(3*3)+(2*3)+(1*9)=86
86 % 10 = 6
So 7403-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3O4/c1-2-5-10-8-4-3-7(11(13)14)6-9(8)12(15)16/h2-4,6,10H,1,5H2

7403-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dinitro-N-prop-2-enylaniline

1.2 Other means of identification

Product number -
Other names N-allyl-2,4-dinitro-aniline

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:7403-39-6 SDS

7403-39-6Relevant articles and documents

Profluorescent substrates for the screening of olefin metathesis catalysts

Reuter, Raphael,Ward, Thomas R.

, p. 1886 - 1892 (2015)

Herein we report on a 96-well plate assay based on the fluorescence resulting from the ring-closing metathesis of two profluorophoric substrates. To demonstrate the validity of the approach, four commercially available ruthenium-metathesis catalysts were

Synthesis and molecular docking for antiinflammatory studies of 2-(arylmethyl)-1-ethyl-1H-benzo[d]imidazol-5-amines

Bucha, Mallaiah,Eppakayala, Laxminarayana,Malothu, Ramesh,Kudle, Karunakar Rao,Merugu, Ramchander

, p. 29 - 33 (2017/12/15)

1-Chloro-2,4-dinitrobenzene (1) was reacted with aliphatic amines (2) in ethanol as solvent under reflux condition for 16-24 h to form N-alkyl-2,4-dinitroaniline (3). Compound 3 undergoes reduction to from N-alkyl-4-nitrobenzene-1,2-diamine (4). Compound 4 was treated with carboxylic acid (5) to offered N-(2-(alkylamino)-5-nitrophenyl)-2-arylacetamide (6) which on cyclization gave 2-(arylmethyl)-1-ethyl-5-nitro-1H-benzo[d]imidazole (7). Finally, compound 7 undergoes reduction give 2-(arylmethyl)-1-ethyl-1H-benzo[d]imidazol-5-amine (8). The synthesized compounds were characterized by using spectral analyses. The compounds synthesized were confirmed by spectral analyses. Molecular docking of 5COX with the ligand using docking server, predicted the compound to be a potential anti-inflammatory compound.

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