Cas 1620004-00-3,N-(2-(4-(2-chlorophenyl)-5-oxa-6-azaspiro[2.4]hept-6-en-7-yl)phenyl)formamide

1620004-00-3

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Basic information

Product Name: N-(2-(4-(2-chlorophenyl)-5-oxa-6-azaspiro[2.4]hept-6-en-7-yl)phenyl)formamide
Synonyms: N-(2-(4-(2-chlorophenyl)-5-oxa-6-azaspiro[2.4]hept-6-en-7-yl)phenyl)formamide
CAS NO:1620004-00-3
Molecular Formula:
Molecular Weight: 326.782
EINECS: N/A
Product Categories: N/A
Mol File: 1620004-00-3.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: N-(2-(4-(2-chlorophenyl)-5-oxa-6-azaspiro[2.4]hept-6-en-7-yl)phenyl)formamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-(4-(2-chlorophenyl)-5-oxa-6-azaspiro[2.4]hept-6-en-7-yl)phenyl)formamide(1620004-00-3)
EPA Substance Registry System: N-(2-(4-(2-chlorophenyl)-5-oxa-6-azaspiro[2.4]hept-6-en-7-yl)phenyl)formamide(1620004-00-3)

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: 1620004-00-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1620004-00-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,0,0 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1620004-00:
(9*1)+(8*6)+(7*2)+(6*0)+(5*0)+(4*0)+(3*4)+(2*0)+(1*0)=83
83 % 10 = 3
So 1620004-00-3 is a valid CAS Registry Number.

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1620004-00-3Relevant articles and documents

An unexpected copper(ii)-catalyzed three-component reaction of quinazoline 3-oxide, alkylidenecyclopropane, and water

An, Yuanyuan,Zheng, Danqing,Wu, Jie

supporting information, p. 9165 - 9167 (2014/08/05)

An unexpected copper(ii)-catalyzed three-component reaction of quinazoline-3-oxide, alkylidenecyclopropane and water under mild conditions is reported. This transformation including [3+2] cycloaddition and intramolecular rearrangement leads to N-(2-(5-oxa

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