Cas 171627-18-2,(2S,3R)-2-tert-Butylsulfanyl-3-hydroxy-3-phenyl-thiopropionic acid S-ethyl ester

171627-18-2

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Basic information

Product Name: (2S,3R)-2-tert-Butylsulfanyl-3-hydroxy-3-phenyl-thiopropionic acid S-ethyl ester
Synonyms:
CAS NO:171627-18-2
Molecular Formula:
Molecular Weight: 298.47
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: (2S,3R)-2-tert-Butylsulfanyl-3-hydroxy-3-phenyl-thiopropionic acid S-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R)-2-tert-Butylsulfanyl-3-hydroxy-3-phenyl-thiopropionic acid S-ethyl ester(171627-18-2)
EPA Substance Registry System: (2S,3R)-2-tert-Butylsulfanyl-3-hydroxy-3-phenyl-thiopropionic acid S-ethyl ester(171627-18-2)

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: 171627-18-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 171627-18-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,6,2 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 171627-18:
(8*1)+(7*7)+(6*1)+(5*6)+(4*2)+(3*7)+(2*1)+(1*8)=132
132 % 10 = 2
So 171627-18-2 is a valid CAS Registry Number.

171627-18-2Upstream product

100-52-7 benzaldehyde

171627-18-2Downstream Products

171627-18-2Relevant academic research and scientific papers

Chiral tin(II) Lewis acid-mediated enantioselective aldol reactions: Synthesis of both enantiomers using similar types of chiral sources

Kobayashi,Horibe

, p. 2565 - 2569 (1995)

Chiral tin(II)-Lewis acid-mediated aldol reactions of various enolates with an aldehyde were investigated by using chiral diamine 2. Based on these reactions, both enantiomers of aldol adducts were prepared using similar types of chiral sources.

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