Cas 916676-24-9,(S)-ETHYL 3-METHYL-2-((R)-3-(3-NITROPHENYL)-5-(PERFLUOROPHENYL)-1,2,4-OXADIAZOL-4(5H)-YL)BUTANOATE

916676-24-9

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Basic information

Product Name: (S)-ETHYL 3-METHYL-2-((R)-3-(3-NITROPHENYL)-5-(PERFLUOROPHENYL)-1,2,4-OXADIAZOL-4(5H)-YL)BUTANOATE
Synonyms: (S)-ETHYL 3-METHYL-2-((R)-3-(3-NITROPHENYL)-5-(PERFLUOROPHENYL)-1,2,4-OXADIAZOL-4(5H)-YL)BUTANOATE
CAS NO:916676-24-9
Molecular Formula: C21H18F5N3O5
Molecular Weight: 487.38
EINECS: N/A
Product Categories: N/A
Mol File: 916676-24-9.mol

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: (S)-ETHYL 3-METHYL-2-((R)-3-(3-NITROPHENYL)-5-(PERFLUOROPHENYL)-1,2,4-OXADIAZOL-4(5H)-YL)BUTANOATE(CAS DataBase Reference)
NIST Chemistry Reference: (S)-ETHYL 3-METHYL-2-((R)-3-(3-NITROPHENYL)-5-(PERFLUOROPHENYL)-1,2,4-OXADIAZOL-4(5H)-YL)BUTANOATE(916676-24-9)
EPA Substance Registry System: (S)-ETHYL 3-METHYL-2-((R)-3-(3-NITROPHENYL)-5-(PERFLUOROPHENYL)-1,2,4-OXADIAZOL-4(5H)-YL)BUTANOATE(916676-24-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 916676-24-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 916676-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,6,7 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 916676-24:
(8*9)+(7*1)+(6*6)+(5*6)+(4*7)+(3*6)+(2*2)+(1*4)=199
199 % 10 = 9
So 916676-24-9 is a valid CAS Registry Number.

916676-24-9Upstream product

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916676-24-9Relevant academic research and scientific papers

Stereoselective preparation of 1,2,4-oxadiazole derivatives substituted by pentafluorophenyl by 1,3-dipolar cycloaddition reaction

Jiang, Huiling,Zhao, Jingwei,Han, Xiaobing,Zhu, Shizheng

, p. 11008 - 11011 (2007/10/03)

1,3-Dipolar cycloaddition reactions of chiral imines obtained from optically active amino acids with nitrile oxides afforded 1,2,4-oxadiazole derivatives in moderate to good yields with good stereoselectivity. Investigation on the effect of bases suggeste

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