Cas 246852-75-5,(1S,3S,4S,5R,6R,8S)-4,5-Bis-benzyloxy-1-methyl-2,7,9,10-tetraoxa-tricyclo[4.3.2.0<sup>3,8</sup>]undecane

246852-75-5

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Basic information

Product Name: (1S,3S,4S,5R,6R,8S)-4,5-Bis-benzyloxy-1-methyl-2,7,9,10-tetraoxa-tricyclo[4.3.2.0^3,8]undecane
Synonyms: (1S,3S,4S,5R,6R,8S)-4,5-Bis-benzyloxy-1-methyl-2,7,9,10-tetraoxa-tricyclo[4.3.2.0^3,8]undecane
CAS NO:246852-75-5
Molecular Formula:
Molecular Weight: 384.429
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: (1S,3S,4S,5R,6R,8S)-4,5-Bis-benzyloxy-1-methyl-2,7,9,10-tetraoxa-tricyclo[4.3.2.0^3,8]undecane(CAS DataBase Reference)
NIST Chemistry Reference: (1S,3S,4S,5R,6R,8S)-4,5-Bis-benzyloxy-1-methyl-2,7,9,10-tetraoxa-tricyclo[4.3.2.0^3,8]undecane(246852-75-5)
EPA Substance Registry System: (1S,3S,4S,5R,6R,8S)-4,5-Bis-benzyloxy-1-methyl-2,7,9,10-tetraoxa-tricyclo[4.3.2.0^3,8]undecane(246852-75-5)

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: 246852-75-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 246852-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,6,8,5 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 246852-75:
(8*2)+(7*4)+(6*6)+(5*8)+(4*5)+(3*2)+(2*7)+(1*5)=165
165 % 10 = 5
So 246852-75-5 is a valid CAS Registry Number.

246852-75-5Upstream product

246852-75-5Downstream Products

119005-82-2 2-O-Acetyl-1,6-anhydro-3,4-di-O-benzyl-β-D-mannopyranose

246852-75-5Relevant academic research and scientific papers

Formation of the 1,2,6-orthoester of mannose and its utilization in the glycosylation reaction

Hiranuma, Sayoko,Kanie, Osamu,Wong, Chi-Huey

, p. 6423 - 6426 (1999)

The synthesis of mannose 1,2,6-orthoester and its utilization in the glycosylation reaction are described.

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