Cas 92808-92-9,tert-Butyl-diphenyl-((2R,3R,4S,5R)-3,4,5-tris-benzyloxy-6-chloro-tetrahydro-pyran-2-ylmethoxy)-silane

92808-92-9

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Basic information

Product Name: tert-Butyl-diphenyl-((2R,3R,4S,5R)-3,4,5-tris-benzyloxy-6-chloro-tetrahydro-pyran-2-ylmethoxy)-silane
Synonyms: tert-Butyl-diphenyl-((2R,3R,4S,5R)-3,4,5-tris-benzyloxy-6-chloro-tetrahydro-pyran-2-ylmethoxy)-silane
CAS NO:92808-92-9
Molecular Formula:
Molecular Weight: 707.382
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: tert-Butyl-diphenyl-((2R,3R,4S,5R)-3,4,5-tris-benzyloxy-6-chloro-tetrahydro-pyran-2-ylmethoxy)-silane(CAS DataBase Reference)
NIST Chemistry Reference: tert-Butyl-diphenyl-((2R,3R,4S,5R)-3,4,5-tris-benzyloxy-6-chloro-tetrahydro-pyran-2-ylmethoxy)-silane(92808-92-9)
EPA Substance Registry System: tert-Butyl-diphenyl-((2R,3R,4S,5R)-3,4,5-tris-benzyloxy-6-chloro-tetrahydro-pyran-2-ylmethoxy)-silane(92808-92-9)

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: 92808-92-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 92808-92-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,0 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92808-92:
(7*9)+(6*2)+(5*8)+(4*0)+(3*8)+(2*9)+(1*2)=159
159 % 10 = 9
So 92808-92-9 is a valid CAS Registry Number.

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92808-92-9Relevant academic research and scientific papers

REACTIONS OF HYDROXYL GROUPS WITH TOSYLCHLORIDE-DIMETHYLAMINOPYRIDINE SYSTEM. DIRECT SYNTHESIS OF CHLORIDES FROM HYDROXYCOMPOUNDS.

Hwang, C. K.,Li, W. S.,Nicolau, K. C.

, p. 2295 - 2296 (1984)

The reactions of various hydroxyl groups with tosylchloride-dimethylaminopyridine system were investigated and direct synthesis of allyl, alkyl and glycosyl chlorides are described.

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