Cas 138607-67-7,(1S,2R,3S,4R,5R)-2-(2-Benzenesulfonyl-ethyl)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]octane

138607-67-7

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Basic information

Product Name: (1S,2R,3S,4R,5R)-2-(2-Benzenesulfonyl-ethyl)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]octane
Synonyms: (1S,2R,3S,4R,5R)-2-(2-Benzenesulfonyl-ethyl)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]octane
CAS NO:138607-67-7
Molecular Formula:
Molecular Weight: 494.609
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,2R,3S,4R,5R)-2-(2-Benzenesulfonyl-ethyl)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]octane(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,3S,4R,5R)-2-(2-Benzenesulfonyl-ethyl)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]octane(138607-67-7)
EPA Substance Registry System: (1S,2R,3S,4R,5R)-2-(2-Benzenesulfonyl-ethyl)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]octane(138607-67-7)

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: 138607-67-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138607-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,0 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 138607-67:
(8*1)+(7*3)+(6*8)+(5*6)+(4*0)+(3*7)+(2*6)+(1*7)=147
147 % 10 = 7
So 138607-67-7 is a valid CAS Registry Number.

138607-67-7Upstream product

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138607-67-7Relevant academic research and scientific papers

Preferred Conformation of C-Glycosides. 8. Synthesis of 1,4-Linked Carbon Disaccharides

Wang, Yuan,Babirad, Stefan A.,Kishi, Yoshito

, p. 468 - 481 (2007/10/02)

Three general synthetic routes to 1,4-linked carbon disaccharides (e.g., 3, 4, 15-17, 21-23, 44, and 45) are presented.Control of the stereochemistry at C.1', C.2', C.5'and C.4, the incorporation of deuterium labels at the C.α position, and structural mod

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