Cas 145742-75-2,1,6-anhydro-3-O-benzoyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-mannopyranose

145742-75-2

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Basic information

Product Name: 1,6-anhydro-3-O-benzoyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-mannopyranose
Synonyms: 1,6-anhydro-3-O-benzoyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-mannopyranose
CAS NO:145742-75-2
Molecular Formula:
Molecular Weight: 596.542
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: 1,6-anhydro-3-O-benzoyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-mannopyranose(CAS DataBase Reference)
NIST Chemistry Reference: 1,6-anhydro-3-O-benzoyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-mannopyranose(145742-75-2)
EPA Substance Registry System: 1,6-anhydro-3-O-benzoyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-mannopyranose(145742-75-2)

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: 145742-75-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 145742-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,7,4 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 145742-75:
(8*1)+(7*4)+(6*5)+(5*7)+(4*4)+(3*2)+(2*7)+(1*5)=142
142 % 10 = 2
So 145742-75-2 is a valid CAS Registry Number.

145742-75-2Upstream product

145742-75-2Downstream Products

145742-76-3 1,6-anhydro-2-azido-3-O-benzoyl-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranose

145742-75-2Relevant academic research and scientific papers

Building blocks for the synthesis of glycosyl-myo-inositols involved in the insulin intracellular signalling process

Zapata, Amparo,Martin-Lomas, Manuel

, p. 93 - 106 (1992)

Glycosylation of (+/-)-1-O-benzyl-2,3:5,6-di-O-isopropylidene-myo-inositol (4) with 6-O-acetyl-4-O-allyl-2-azido-3-O-benzyl-2-deoxy-β-D-glucopyranosyl trichloroacetimidate (6) gave the 4-O-(2-amino-2-deoxy-α-D-glucopyranosyl)-myo-inositol derivative (9) a

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