Cas 1040741-68-1,2-[allyl-(3-iodo-5-nitro-pyridin-2-yl)-amino]-4-methyl-pentanoic acid 4-chlorobenzylamide

1040741-68-1

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Basic information

Product Name: 2-[allyl-(3-iodo-5-nitro-pyridin-2-yl)-amino]-4-methyl-pentanoic acid 4-chlorobenzylamide
Synonyms: 2-[allyl-(3-iodo-5-nitro-pyridin-2-yl)-amino]-4-methyl-pentanoic acid 4-chlorobenzylamide
CAS NO:1040741-68-1
Molecular Formula:
Molecular Weight: 542.804
EINECS: N/A
Product Categories: N/A
Mol File: 1040741-68-1.mol
Article Data: 1

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: 2-[allyl-(3-iodo-5-nitro-pyridin-2-yl)-amino]-4-methyl-pentanoic acid 4-chlorobenzylamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-[allyl-(3-iodo-5-nitro-pyridin-2-yl)-amino]-4-methyl-pentanoic acid 4-chlorobenzylamide(1040741-68-1)
EPA Substance Registry System: 2-[allyl-(3-iodo-5-nitro-pyridin-2-yl)-amino]-4-methyl-pentanoic acid 4-chlorobenzylamide(1040741-68-1)

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: 1040741-68-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1040741-68-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,0,7,4 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1040741-68:
(9*1)+(8*0)+(7*4)+(6*0)+(5*7)+(4*4)+(3*1)+(2*6)+(1*8)=111
111 % 10 = 1
So 1040741-68-1 is a valid CAS Registry Number.

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1040741-68-1Relevant articles and documents

New MCR-Heck-isomerization cascade toward indoles

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

supporting information; experimental part, p. 3417 - 3419 (2009/05/07)

(Chemical Equation Presented) The use of ortho-iodonitrophenol in Ugi-Smiles reaction coupled with Heck cyclization gives new access to indole scaffolds. The sequence can be performed in a one-pot reaction if the residual isocyanide is neutralized prior to the addition of the palladium catalyst.

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