Cas 1432726-71-0,(E)-N-(5-chloro-2-iodophenyl)-N-[1-(phenylsulfonyl)pent-2-en-2-yl]formamide

1432726-71-0

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Basic information

Product Name: (E)-N-(5-chloro-2-iodophenyl)-N-[1-(phenylsulfonyl)pent-2-en-2-yl]formamide
Synonyms: (E)-N-(5-chloro-2-iodophenyl)-N-[1-(phenylsulfonyl)pent-2-en-2-yl]formamide
CAS NO:1432726-71-0
Molecular Formula:
Molecular Weight: 489.761
EINECS: N/A
Product Categories: N/A
Mol File: 1432726-71-0.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: (E)-N-(5-chloro-2-iodophenyl)-N-[1-(phenylsulfonyl)pent-2-en-2-yl]formamide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-N-(5-chloro-2-iodophenyl)-N-[1-(phenylsulfonyl)pent-2-en-2-yl]formamide(1432726-71-0)
EPA Substance Registry System: (E)-N-(5-chloro-2-iodophenyl)-N-[1-(phenylsulfonyl)pent-2-en-2-yl]formamide(1432726-71-0)

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: 1432726-71-0(Hazardous Substances Data)

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1432726-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1432726-71-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,2,7,2 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1432726-71:
(9*1)+(8*4)+(7*3)+(6*2)+(5*7)+(4*2)+(3*6)+(2*7)+(1*1)=150
150 % 10 = 0
So 1432726-71-0 is a valid CAS Registry Number.

1432726-71-0Upstream product

1432726-71-0Downstream Products

1432726-77-6 C₁₈H₁₇ClINO₃S

1432726-71-0Relevant articles and documents

Indole synthesis by conjugate addition of anilines to activated acetylenes and an unusual ligand-free copper(II)-mediated intramolecular cross-coupling

Gao, Detian,Back, Thomas G.

, p. 14828 - 14840 (2013/01/15)

A versatile new synthesis of indoles was achieved by the conjugate addition of N-formyl-2-haloanilines to acetylenic sulfones, ketones, and esters followed by a copper-catalyzed intramolecular C-arylation. The conjugate addition step was conducted under e

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