Cas 696599-10-7,2-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-β-D-mannopyranosyl-(1->4)-2-O-allyl-3,6-di-O-benzyl-β-D-galactopyranoside

696599-10-7

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Basic information

Product Name: 2-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-β-D-mannopyranosyl-(1->4)-2-O-allyl-3,6-di-O-benzyl-β-D-galactopyranoside
Synonyms: 2-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-β-D-mannopyranosyl-(1->4)-2-O-allyl-3,6-di-O-benzyl-β-D-galactopyranoside
CAS NO:696599-10-7
Molecular Formula:
Molecular Weight: 933.224
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-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-β-D-mannopyranosyl-(1->4)-2-O-allyl-3,6-di-O-benzyl-β-D-galactopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 2-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-β-D-mannopyranosyl-(1->4)-2-O-allyl-3,6-di-O-benzyl-β-D-galactopyranoside(696599-10-7)
EPA Substance Registry System: 2-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-β-D-mannopyranosyl-(1->4)-2-O-allyl-3,6-di-O-benzyl-β-D-galactopyranoside(696599-10-7)

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: 696599-10-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 696599-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,6,5,9 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 696599-10:
(8*6)+(7*9)+(6*6)+(5*5)+(4*9)+(3*9)+(2*1)+(1*0)=237
237 % 10 = 7
So 696599-10-7 is a valid CAS Registry Number.

696599-10-7Upstream product

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696599-10-7Relevant academic research and scientific papers

Synthesis of a Tetrasaccharide Related to the Repeating Unit of the Antigen from Shigella dysenteriae Type 9 in the Form of Its 2-(Trimethylsilyl)ethyl Glycoside

Roy, Samarpita,Sarkar, Sujit Kumar,Roy, Nirmolendu

, p. 1125 - 1139 (2007/10/03)

Starting from D-mannose, D-galactose and D-glucosamine hydrochloride, two disaccharide blocks were synthesized. Schmidt's inverse addition technique for trichloroacetimidate was utilized for the construction of a disaccharide with a β-mannosidic linkage i

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