Cas 727671-45-6,N-[3-(2-oxopropyl)-1,2,4-thiadiazol-5-yl]-5-(2-trifluoromethylphenyl)furan-2-carboxamide

727671-45-6

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Basic information

Product Name: N-[3-(2-oxopropyl)-1,2,4-thiadiazol-5-yl]-5-(2-trifluoromethylphenyl)furan-2-carboxamide
Synonyms:
CAS NO:727671-45-6
Molecular Formula:
Molecular Weight: 395.362
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: N-[3-(2-oxopropyl)-1,2,4-thiadiazol-5-yl]-5-(2-trifluoromethylphenyl)furan-2-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[3-(2-oxopropyl)-1,2,4-thiadiazol-5-yl]-5-(2-trifluoromethylphenyl)furan-2-carboxamide(727671-45-6)
EPA Substance Registry System: N-[3-(2-oxopropyl)-1,2,4-thiadiazol-5-yl]-5-(2-trifluoromethylphenyl)furan-2-carboxamide(727671-45-6)

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: 727671-45-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 727671-45-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,7,6,7 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 727671-45:
(8*7)+(7*2)+(6*7)+(5*6)+(4*7)+(3*1)+(2*4)+(1*5)=186
186 % 10 = 6
So 727671-45-6 is a valid CAS Registry Number.

727671-45-6Upstream product

1072-67-9 5-methylisoxazol-3-ylamine

727671-45-6Downstream Products

727671-45-6Relevant academic research and scientific papers

Synthesis of heterocycles from arylation products of unsaturated compounds: XVIII. 5-Arylfuran-2-carboxylic acids and their application in the synthesis of 1,2,4-thiadiazole, 1,3,4-oxadiazole, and [1,2,4]triazolo[3,4-b][1,3,4] thiadiazole derivatives

Gorak,Obushak,Matiichuk,Lytvyn

, p. 541 - 550 (2009)

Arylation of furan-2-carboxylic acid or its methyl ester with arenediazonium chlorides in the presence of copper(II) chloride gave the corresponding 5-arylfuran-2-carboxylic acids or methyl 5-arylfuran-2- carboxylates. 5-Arylfuran-2-carbonyl chlorides rea

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