Cas 850733-75-4,(S)-4-Isopropyl-3-((1S,2R)-2-mercapto-cyclohexanecarbonyl)-5,5-dimethyl-oxazolidin-2-one

850733-75-4

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Basic information

Product Name: (S)-4-Isopropyl-3-((1S,2R)-2-mercapto-cyclohexanecarbonyl)-5,5-dimethyl-oxazolidin-2-one
Synonyms: (S)-4-Isopropyl-3-((1S,2R)-2-mercapto-cyclohexanecarbonyl)-5,5-dimethyl-oxazolidin-2-one
CAS NO:850733-75-4
Molecular Formula:
Molecular Weight: 299.434
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)-4-Isopropyl-3-((1S,2R)-2-mercapto-cyclohexanecarbonyl)-5,5-dimethyl-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-Isopropyl-3-((1S,2R)-2-mercapto-cyclohexanecarbonyl)-5,5-dimethyl-oxazolidin-2-one(850733-75-4)
EPA Substance Registry System: (S)-4-Isopropyl-3-((1S,2R)-2-mercapto-cyclohexanecarbonyl)-5,5-dimethyl-oxazolidin-2-one(850733-75-4)

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: 850733-75-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 850733-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,7,3 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 850733-75:
(8*8)+(7*5)+(6*0)+(5*7)+(4*3)+(3*3)+(2*7)+(1*5)=174
174 % 10 = 4
So 850733-75-4 is a valid CAS Registry Number.

850733-75-4Upstream product

850733-75-4Downstream Products

850733-80-1 (S)-4-Isopropyl-5,5-dimethyl-3-((1S,2R)-2-methylsulfanyl-cyclohexanecarbonyl)-oxazolidin-2-one

850733-75-4Relevant academic research and scientific papers

Asymmetric synthesis of 3-methylthio alcohols by intramolecular Michael addition reactions

Ortiz, Aurelio,Hernández, Hector,Mendoza, Guadalupe,Quintero, Leticia,Bernès, Sylvain

, p. 2243 - 2246 (2005)

Chiral 3-methylthio alcohols have been synthesized through a known intramolecular sulfur transfer reaction that has been carried out in di- and trisubstituted α,β-unsaturated N-enoyl oxazolidinethiones as substrates, giving rise to syn/anti-diastereomers. The anti-diastereomer is favored and obtained via a highly diastereoselective protonation step.

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