Cas 845532-36-7,6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl-(1->6)-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate

845532-36-7

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Basic information

Product Name: 6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl-(1->6)-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate
Synonyms: 6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl-(1->6)-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate
CAS NO:845532-36-7
Molecular Formula:
Molecular Weight: 1153.37
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: 6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl-(1->6)-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate(CAS DataBase Reference)
NIST Chemistry Reference: 6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl-(1->6)-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate(845532-36-7)
EPA Substance Registry System: 6-O-acetyl-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl-(1->6)-2,3,5-tri-O-benzoyl-β-D-galactofuranosyl trichloroacetimidate(845532-36-7)

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: 845532-36-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 845532-36-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,5,3 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 845532-36:
(8*8)+(7*4)+(6*5)+(5*5)+(4*3)+(3*2)+(2*3)+(1*6)=177
177 % 10 = 7
So 845532-36-7 is a valid CAS Registry Number.

845532-36-7Upstream product

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845532-36-7Relevant academic research and scientific papers

An efficient and concise synthesis of a β-(1→6)-linked d-galactofuranosyl hexasaccharide

Zhang, Guohua,Fu, Mingkun,Ning, Jun

, p. 155 - 159 (2007/10/03)

A β-(1→6)-linked d-galactofuranosyl hexasaccharide was synthesized efficiently in a block construction manner by the well-known Schmidt glycosylation method using 6-O-acetyl-2,3,5-tri-O-benzoyl-β-d- galactofuranosyl trichloroacetimidate (1) and allyl 2,3,

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