Cas 208335-80-2,5-[2-(3,4-dimethoxyphenyl)acetylamino]furan-2-carboxylic acid methyl ester

208335-80-2

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Basic information

Product Name: 5-[2-(3,4-dimethoxyphenyl)acetylamino]furan-2-carboxylic acid methyl ester
Synonyms: 5-[2-(3,4-dimethoxyphenyl)acetylamino]furan-2-carboxylic acid methyl ester
CAS NO:208335-80-2
Molecular Formula:
Molecular Weight: 319.314
EINECS: N/A
Product Categories: N/A

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: 5-[2-(3,4-dimethoxyphenyl)acetylamino]furan-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-[2-(3,4-dimethoxyphenyl)acetylamino]furan-2-carboxylic acid methyl ester(208335-80-2)
EPA Substance Registry System: 5-[2-(3,4-dimethoxyphenyl)acetylamino]furan-2-carboxylic acid methyl ester(208335-80-2)

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: 208335-80-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 208335-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,3,3 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 208335-80:
(8*2)+(7*0)+(6*8)+(5*3)+(4*3)+(3*5)+(2*8)+(1*0)=122
122 % 10 = 2
So 208335-80-2 is a valid CAS Registry Number.

208335-80-2Upstream product

208335-80-2Downstream Products

208335-24-4 5-[[2-(3,4-Dimethoxy-phenyl)-acetyl]-(3-methyl-but-3-enyl)-amino]-furan-2-carboxylic acid methyl ester

208335-80-2Relevant academic research and scientific papers

IMDAF Cycloaddition as a Method for the Preparation of Pyrrolophenanthridine Alkaloids

Padwa, Albert,Dimitroff, Martin,Waterson, Alex G.,Wu, Tianhua

, p. 3986 - 3997 (1998)

Acylation of 5-amino-2-furancarboxylic acid methyl ester with alkenoyl acid chlorides gives 2-amidofurans that undergo intramolecular Diels-Alder cycloadditions. The reactions occur at 165°C in toluene or at 100°C when 4 M ethereal LiClO4 was u

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