Cas 952575-74-5,2-O-benzyl-3,5-O-(di-tert-butylsilanediyl)-α-L-arabinifuranosyl trichloroacetimidate

952575-74-5

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Basic information

Product Name: 2-O-benzyl-3,5-O-(di-tert-butylsilanediyl)-α-L-arabinifuranosyl trichloroacetimidate
Synonyms: 2-O-benzyl-3,5-O-(di-tert-butylsilanediyl)-α-L-arabinifuranosyl trichloroacetimidate
CAS NO:952575-74-5
Molecular Formula:
Molecular Weight: 524.944
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: 2-O-benzyl-3,5-O-(di-tert-butylsilanediyl)-α-L-arabinifuranosyl trichloroacetimidate(CAS DataBase Reference)
NIST Chemistry Reference: 2-O-benzyl-3,5-O-(di-tert-butylsilanediyl)-α-L-arabinifuranosyl trichloroacetimidate(952575-74-5)
EPA Substance Registry System: 2-O-benzyl-3,5-O-(di-tert-butylsilanediyl)-α-L-arabinifuranosyl trichloroacetimidate(952575-74-5)

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: 952575-74-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 952575-74-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,2,5,7 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 952575-74:
(8*9)+(7*5)+(6*2)+(5*5)+(4*7)+(3*5)+(2*7)+(1*4)=205
205 % 10 = 5
So 952575-74-5 is a valid CAS Registry Number.

952575-74-5Upstream product

545-06-2 trichloroacetonitrile

952575-74-5Downstream Products

952575-81-4 phenyl 2-O-benzyl-3,5-O-(di-tert-butylsilane-diyl)-β-L-arabinofuranosyl-(1->3)-2,4-di-O-benzoyl-1-thio-α-L-rhamnopyranoside

952575-74-5Relevant academic research and scientific papers

A highly convergent chemical synthesis of conformational epitopes of rhamnogalacturonan II

Rao, Yu,Boons, Geert-Jan

, p. 6148 - 6151 (2007)

(Chemical Equation Presented) Upon careful tuning of the reactivity of glycosyl donors and acceptors, tetra- and hexasaccharide fragments (see structure) of the B chain of rhamnogalacturonan II (RGII) were prepared in a convergent and stereoselective mann

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