Cas 105165-75-1,Acetic acid (2S,3S,4R,5R)-4-acetoxy-2-((1R,2R,4R,5S,6R)-5-acetoxy-2-trityloxymethyl-3,7-dioxa-bicyclo[4.1.0]hept-4-yloxy)-2,5-bis-trityloxymethyl-tetrahydro-furan-3-yl ester

105165-75-1

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Basic information

Product Name: Acetic acid (2S,3S,4R,5R)-4-acetoxy-2-((1R,2R,4R,5S,6R)-5-acetoxy-2-trityloxymethyl-3,7-dioxa-bicyclo[4.1.0]hept-4-yloxy)-2,5-bis-trityloxymethyl-tetrahydro-furan-3-yl ester
Synonyms:
CAS NO:105165-75-1
Molecular Formula:
Molecular Weight: 1177.36
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: Acetic acid (2S,3S,4R,5R)-4-acetoxy-2-((1R,2R,4R,5S,6R)-5-acetoxy-2-trityloxymethyl-3,7-dioxa-bicyclo[4.1.0]hept-4-yloxy)-2,5-bis-trityloxymethyl-tetrahydro-furan-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2S,3S,4R,5R)-4-acetoxy-2-((1R,2R,4R,5S,6R)-5-acetoxy-2-trityloxymethyl-3,7-dioxa-bicyclo[4.1.0]hept-4-yloxy)-2,5-bis-trityloxymethyl-tetrahydro-furan-3-yl ester(105165-75-1)
EPA Substance Registry System: Acetic acid (2S,3S,4R,5R)-4-acetoxy-2-((1R,2R,4R,5S,6R)-5-acetoxy-2-trityloxymethyl-3,7-dioxa-bicyclo[4.1.0]hept-4-yloxy)-2,5-bis-trityloxymethyl-tetrahydro-furan-3-yl ester(105165-75-1)

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: 105165-75-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 105165-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,1,6 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 105165-75:
(8*1)+(7*0)+(6*5)+(5*1)+(4*6)+(3*5)+(2*7)+(1*5)=101
101 % 10 = 1
So 105165-75-1 is a valid CAS Registry Number.

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105165-75-1Relevant academic research and scientific papers

PREPARATION AND RING-OPENING REACTIONS OF A 2,3-ANHYDRIDE DERIVED FROM SUCROSE

Gurjar, Mukund K.,Hough, Leslie,Richardson, Anthony C.,Sincharoenkul, Lee V.

, p. 53 - 62 (2007/10/02)

Selective tosylation of 6,1',6'-tri-O-tritylsucrose afforded the 2-O-tosyl derivative and not the 3-O-tosyl derivative as previously claimed.Treatment of the 2-tosylate with base afforded mainly (40percent) the 2,3-manno-epoxide together with the 3,4-altr

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