Cas 14668-50-9,N-(2-methoxyphenyl)-2-oxotetrahydro-3-furancarboxamide

14668-50-9

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Basic information

Product Name: N-(2-methoxyphenyl)-2-oxotetrahydro-3-furancarboxamide
Synonyms: N-(2-methoxyphenyl)-2-oxotetrahydro-3-furancarboxamide
CAS NO:14668-50-9
Molecular Formula: C12H13NO4
Molecular Weight: 235.23592
EINECS: N/A
Product Categories: N/A
Mol File: 14668-50-9.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-(2-methoxyphenyl)-2-oxotetrahydro-3-furancarboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-methoxyphenyl)-2-oxotetrahydro-3-furancarboxamide(14668-50-9)
EPA Substance Registry System: N-(2-methoxyphenyl)-2-oxotetrahydro-3-furancarboxamide(14668-50-9)

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: 14668-50-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 14668-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,6 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14668-50:
(7*1)+(6*4)+(5*6)+(4*6)+(3*8)+(2*5)+(1*0)=119
119 % 10 = 9
So 14668-50-9 is a valid CAS Registry Number.

14668-50-9Upstream product

1373611-08-5 N-(2-methoxyphenyl)cyclopropane-1,1-dicarboxamide

14668-50-9Downstream Products

14668-50-9Relevant articles and documents

Formal [4+1] annulation of cyclopropyl amides and water mediated by Lewis acid: A novel entry to γ-butyrolactones

Zhang, Dingyuan,Zhang, Rui,Liang, Yongjiu,Dong, Dewen

experimental part, p. 1679 - 1685 (2012/07/03)

An efficient one-pot synthesis of substituted -butyrolactones from cyclopropyl amides mediated by the Lewis acid SnClH is reported. A mechanism involving a tandem ring-opening reaction and intramolecular cyclization reaction is proposed. Georg Thieme Verlag Stuttgart · New York.

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