Cas 107041-74-7,5,5-Dimethyl-4-phenylsulfanyl-3-(4-trimethylsilanyl-but-3-ynyl)-oxazolidin-2-one

107041-74-7

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Basic information

Product Name: 5,5-Dimethyl-4-phenylsulfanyl-3-(4-trimethylsilanyl-but-3-ynyl)-oxazolidin-2-one
Synonyms:
CAS NO:107041-74-7
Molecular Formula:
Molecular Weight: 347.553
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: 5,5-Dimethyl-4-phenylsulfanyl-3-(4-trimethylsilanyl-but-3-ynyl)-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 5,5-Dimethyl-4-phenylsulfanyl-3-(4-trimethylsilanyl-but-3-ynyl)-oxazolidin-2-one(107041-74-7)
EPA Substance Registry System: 5,5-Dimethyl-4-phenylsulfanyl-3-(4-trimethylsilanyl-but-3-ynyl)-oxazolidin-2-one(107041-74-7)

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: 107041-74-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 107041-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,4 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 107041-74:
(8*1)+(7*0)+(6*7)+(5*0)+(4*4)+(3*1)+(2*7)+(1*4)=87
87 % 10 = 7
So 107041-74-7 is a valid CAS Registry Number.

107041-74-7Upstream product

107041-66-7 5,5-Dimethyl-3-(4-trimethylsilanyl-but-3-ynyl)-oxazolidine-2,4-dione

107041-74-7Downstream Products

107041-74-7Relevant academic research and scientific papers

α-ACYLAMINORADICAL ANNELATION IN THE DIASTEREOSELECTIVE SYNTHESIS OF 1- AND 5-SUBSTITUTED TETRAHYDROPYRROLOOXAZOLE AND 1-SUBSTITUTED PYRROLIZIDINE DERIVATIVES

Kano, Shinzo,Yuasa, Yoko,Asami, Kenji,Shibuya, Shiroshi

, p. 735 - 736 (1986)

Diastereoselective synthesis of 1,8-trans-1-substituted and 5,8-trans-5-substituted tetrahydropyrrolooxazoles was achieved by an application of α-acylaminoradical cyclization at a silylated triple bond.The method was applied to an enantioselective

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