Cas 358681-52-4,(2R,4S,5R,6R)-5-Acetylamino-4-benzyloxy-2-p-tolylsulfanyl-6-((1S,2R)-1,2,3-tris-benzyloxy-propyl)-tetrahydro-pyran-2-carboxylic acid benzyl ester

358681-52-4

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Basic information

Product Name: (2R,4S,5R,6R)-5-Acetylamino-4-benzyloxy-2-p-tolylsulfanyl-6-((1S,2R)-1,2,3-tris-benzyloxy-propyl)-tetrahydro-pyran-2-carboxylic acid benzyl ester
Synonyms: (2R,4S,5R,6R)-5-Acetylamino-4-benzyloxy-2-p-tolylsulfanyl-6-((1S,2R)-1,2,3-tris-benzyloxy-propyl)-tetrahydro-pyran-2-carboxylic acid benzyl ester
CAS NO:358681-52-4
Molecular Formula:
Molecular Weight: 866.088
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: (2R,4S,5R,6R)-5-Acetylamino-4-benzyloxy-2-p-tolylsulfanyl-6-((1S,2R)-1,2,3-tris-benzyloxy-propyl)-tetrahydro-pyran-2-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,4S,5R,6R)-5-Acetylamino-4-benzyloxy-2-p-tolylsulfanyl-6-((1S,2R)-1,2,3-tris-benzyloxy-propyl)-tetrahydro-pyran-2-carboxylic acid benzyl ester(358681-52-4)
EPA Substance Registry System: (2R,4S,5R,6R)-5-Acetylamino-4-benzyloxy-2-p-tolylsulfanyl-6-((1S,2R)-1,2,3-tris-benzyloxy-propyl)-tetrahydro-pyran-2-carboxylic acid benzyl ester(358681-52-4)

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: 358681-52-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 358681-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,8,6,8 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 358681-52:
(8*3)+(7*5)+(6*8)+(5*6)+(4*8)+(3*1)+(2*5)+(1*2)=184
184 % 10 = 4
So 358681-52-4 is a valid CAS Registry Number.

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358681-52-4Relevant academic research and scientific papers

Conversion of the carboxy group of sialic acid donors to a protected hydroxymethyl group yields an efficient reagent for the synthesis of the unnatural beta-linkage

Ye,Huang,Wong

, p. 974 - 975 (2001)

New sialyl donors with a protected hydroxymethyl group at the anomeric center are over 1000 times more reactive than the normal ester containing sialylation reagent and give excellent yield (> 90%) with unusually high β-stereoselectivity in sialylation.

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