Cas 1344031-41-9,(S)-2-(3,5-diethoxyphenyl)-4-phenyl-4-((R)-2,4,4-trimethyltetrahydrofuran-2-yl)oxazol-5(4H)-one

1344031-41-9

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Basic information

Product Name: (S)-2-(3,5-diethoxyphenyl)-4-phenyl-4-((R)-2,4,4-trimethyltetrahydrofuran-2-yl)oxazol-5(4H)-one
Synonyms: (S)-2-(3,5-diethoxyphenyl)-4-phenyl-4-((R)-2,4,4-trimethyltetrahydrofuran-2-yl)oxazol-5(4H)-one
CAS NO:1344031-41-9
Molecular Formula:
Molecular Weight: 437.536
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: (S)-2-(3,5-diethoxyphenyl)-4-phenyl-4-((R)-2,4,4-trimethyltetrahydrofuran-2-yl)oxazol-5(4H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-(3,5-diethoxyphenyl)-4-phenyl-4-((R)-2,4,4-trimethyltetrahydrofuran-2-yl)oxazol-5(4H)-one(1344031-41-9)
EPA Substance Registry System: (S)-2-(3,5-diethoxyphenyl)-4-phenyl-4-((R)-2,4,4-trimethyltetrahydrofuran-2-yl)oxazol-5(4H)-one(1344031-41-9)

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: 1344031-41-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1344031-41-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,4,0,3 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1344031-41:
(9*1)+(8*3)+(7*4)+(6*4)+(5*0)+(4*3)+(3*1)+(2*4)+(1*1)=109
109 % 10 = 9
So 1344031-41-9 is a valid CAS Registry Number.

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1344031-41-9Relevant academic research and scientific papers

Enantioselective concomitant creation of vicinal quaternary stereogenic centers via cyclization of alkynols triggered addition of azlactones

Han, Zhi-Yong,Guo, Rui,Wang, Pu-Sheng,Chen, Dian-Feng,Xiao, Han,Gong, Liu-Zhu

, p. 5963 - 5967 (2011)

An asymmetric cyclization of alkynols triggered addition of azlactones catalyzed by a combined catalyst system consisting of a chiral gold phosphate and a phosphoric acid produces conformationally restricted amino acid precursors bearing vicinal quaternar

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