Cas 153541-54-9,Acetic acid (2R,3R,4S,5R)-3-acetoxy-2-acetoxymethyl-5-(chloro-dimethyl-silanyloxy)-6-phenylsulfanyl-tetrahydro-pyran-4-yl ester

153541-54-9

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Basic information

Product Name: Acetic acid (2R,3R,4S,5R)-3-acetoxy-2-acetoxymethyl-5-(chloro-dimethyl-silanyloxy)-6-phenylsulfanyl-tetrahydro-pyran-4-yl ester
Synonyms:
CAS NO:153541-54-9
Molecular Formula:
Molecular Weight: 491.034
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: Acetic acid (2R,3R,4S,5R)-3-acetoxy-2-acetoxymethyl-5-(chloro-dimethyl-silanyloxy)-6-phenylsulfanyl-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3R,4S,5R)-3-acetoxy-2-acetoxymethyl-5-(chloro-dimethyl-silanyloxy)-6-phenylsulfanyl-tetrahydro-pyran-4-yl ester(153541-54-9)
EPA Substance Registry System: Acetic acid (2R,3R,4S,5R)-3-acetoxy-2-acetoxymethyl-5-(chloro-dimethyl-silanyloxy)-6-phenylsulfanyl-tetrahydro-pyran-4-yl ester(153541-54-9)

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: 153541-54-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 153541-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,5,4 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 153541-54:
(8*1)+(7*5)+(6*3)+(5*5)+(4*4)+(3*1)+(2*5)+(1*4)=119
119 % 10 = 9
So 153541-54-9 is a valid CAS Registry Number.

153541-54-9Upstream product

75-78-5 dimethylsilicon dichloride

153541-54-9Downstream Products

153541-54-9Relevant academic research and scientific papers

Application of Intramolecular Glycosidation to the Stereocontrolled Synthesis of Disaccharides containing α-Gluco and α-Galacto Linkages

Bols, Mikael

, p. 791 - 792 (1993)

Disaccharides containing α-glucose and α-galactose linkages are stereospecifically synthesized from primary and secondary sugar hydroxy groups and a 2-hydroxythioglycoside via intramolecular glycosidation of a dimethylsilyl tethered intermediate.

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