Cas 331268-34-9,phenyl 1-thio-2-O-benzyl-3-O-(tert-butyldimethylsilyl)-4-O-(tert-butyldiphenylsilyl)-α-L-rhamnopyranoside

331268-34-9

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Basic information

Product Name: phenyl 1-thio-2-O-benzyl-3-O-(tert-butyldimethylsilyl)-4-O-(tert-butyldiphenylsilyl)-α-L-rhamnopyranoside
Synonyms: phenyl 1-thio-2-O-benzyl-3-O-(tert-butyldimethylsilyl)-4-O-(tert-butyldiphenylsilyl)-α-L-rhamnopyranoside
CAS NO:331268-34-9
Molecular Formula:
Molecular Weight: 699.114
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: phenyl 1-thio-2-O-benzyl-3-O-(tert-butyldimethylsilyl)-4-O-(tert-butyldiphenylsilyl)-α-L-rhamnopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: phenyl 1-thio-2-O-benzyl-3-O-(tert-butyldimethylsilyl)-4-O-(tert-butyldiphenylsilyl)-α-L-rhamnopyranoside(331268-34-9)
EPA Substance Registry System: phenyl 1-thio-2-O-benzyl-3-O-(tert-butyldimethylsilyl)-4-O-(tert-butyldiphenylsilyl)-α-L-rhamnopyranoside(331268-34-9)

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: 331268-34-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 331268-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,2,6 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 331268-34:
(8*3)+(7*3)+(6*1)+(5*2)+(4*6)+(3*8)+(2*3)+(1*4)=119
119 % 10 = 9
So 331268-34-9 is a valid CAS Registry Number.

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331268-34-9Relevant academic research and scientific papers

Rhamnosylation reaction with a phenyl 1-thiorhamnoside and a rhamnosyl fluoride which have 4C1 conformation

Yamada, Hidetoshi,Ikeda, Tomonari

, p. 432 - 433 (2000)

Rhamnosylation reaction with a phenyl 1-thiorhamnoside and a rhamnosyl fluoride that has chair conformation with more axial substituents (4C1) is described. Flipping of the ring conformation changed the high α-selectivity of the gene

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