Cas 1007383-10-9,N-(4-chlorobenzyl)-2-[N-(4-chlorobenzyl)-4-(6-chloro-2-iodo-4-nitrophenyl)amino]-4-methylpentanamide

1007383-10-9

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Basic information

Product Name: N-(4-chlorobenzyl)-2-[N-(4-chlorobenzyl)-4-(6-chloro-2-iodo-4-nitrophenyl)amino]-4-methylpentanamide
Synonyms: N-(4-chlorobenzyl)-2-[N-(4-chlorobenzyl)-4-(6-chloro-2-iodo-4-nitrophenyl)amino]-4-methylpentanamide
CAS NO:1007383-10-9
Molecular Formula:
Molecular Weight: 660.766
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-(4-chlorobenzyl)-2-[N-(4-chlorobenzyl)-4-(6-chloro-2-iodo-4-nitrophenyl)amino]-4-methylpentanamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(4-chlorobenzyl)-2-[N-(4-chlorobenzyl)-4-(6-chloro-2-iodo-4-nitrophenyl)amino]-4-methylpentanamide(1007383-10-9)
EPA Substance Registry System: N-(4-chlorobenzyl)-2-[N-(4-chlorobenzyl)-4-(6-chloro-2-iodo-4-nitrophenyl)amino]-4-methylpentanamide(1007383-10-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1007383-10-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1007383-10-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,3,8 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1007383-10:
(9*1)+(8*0)+(7*0)+(6*7)+(5*3)+(4*8)+(3*3)+(2*1)+(1*0)=109
109 % 10 = 9
So 1007383-10-9 is a valid CAS Registry Number.

1007383-10-9Upstream product

1007383-10-9Downstream Products

1007383-15-4 5-chloro-1,4-bis(4-chlorobenzyl)-3-isobutyl-7-nitro-3,4-dihydroquinoxalin-2(1H)-one

1007383-10-9Relevant academic research and scientific papers

Ugi-smiles access to quinoxaline derivatives

Oble, Julie,El Kaim, Laurent,Gizzi, Marion,Grimaud, Laurence

, p. 503 - 517 (2007)

Two different Ugi-Smiles post-condensations strategies have been used for new three and four-component formation of quinoxaline scaffolds. In the first approach, a one-pot hydrogenation-cyclization affords the heterocycle with loss of the initial isocyani

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