Cas 1360703-69-0,(Z)-3-benzoyl-5,5-dimethyl-4-(thiophene-2-ylmethylene)oxazolidin-2-one

1360703-69-0

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Basic information

Product Name: (Z)-3-benzoyl-5,5-dimethyl-4-(thiophene-2-ylmethylene)oxazolidin-2-one
Synonyms: (Z)-3-benzoyl-5,5-dimethyl-4-(thiophene-2-ylmethylene)oxazolidin-2-one
CAS NO:1360703-69-0
Molecular Formula:
Molecular Weight: 313.377
EINECS: N/A
Product Categories: N/A
Mol File: 1360703-69-0.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: (Z)-3-benzoyl-5,5-dimethyl-4-(thiophene-2-ylmethylene)oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-3-benzoyl-5,5-dimethyl-4-(thiophene-2-ylmethylene)oxazolidin-2-one(1360703-69-0)
EPA Substance Registry System: (Z)-3-benzoyl-5,5-dimethyl-4-(thiophene-2-ylmethylene)oxazolidin-2-one(1360703-69-0)

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: 1360703-69-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1360703-69-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,7,0 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1360703-69:
(9*1)+(8*3)+(7*6)+(6*0)+(5*7)+(4*0)+(3*3)+(2*6)+(1*9)=140
140 % 10 = 0
So 1360703-69-0 is a valid CAS Registry Number.

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1360703-69-0Relevant articles and documents

N -heterocyclic carbene catalyzed domino cyclization of propargylic alcohols and benzoyl isocyanates

Jo, Kyoung A.,Maheswara, Muchchintala,Yoon, Eunyoung,Lee, Yun Yeong,Yun, Hoseop,Kang, Eun Joo

experimental part, p. 2924 - 2928 (2012/05/04)

N-Hetereocyclic carbenes (NHCs) were found to be efficient catalysts for the cyclization of propargylic alcohols and isocyanates. Domino cyclization reactions were carried out using isopropyl-substituted imidazolium salt as a precatalyst, and a wide range

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