Cas 64035-99-0,benzyl 5-O-(2,3-dideoxy-α-DL-threo-hex-2-enopyranosyl)-2,3-O-isopropylidene-β-D-ribofuranoside

64035-99-0

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Basic information

Product Name: benzyl 5-O-(2,3-dideoxy-α-DL-threo-hex-2-enopyranosyl)-2,3-O-isopropylidene-β-D-ribofuranoside
Synonyms: benzyl 5-O-(2,3-dideoxy-α-DL-threo-hex-2-enopyranosyl)-2,3-O-isopropylidene-β-D-ribofuranoside
CAS NO:64035-99-0
Molecular Formula:
Molecular Weight: 408.449
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: benzyl 5-O-(2,3-dideoxy-α-DL-threo-hex-2-enopyranosyl)-2,3-O-isopropylidene-β-D-ribofuranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 5-O-(2,3-dideoxy-α-DL-threo-hex-2-enopyranosyl)-2,3-O-isopropylidene-β-D-ribofuranoside(64035-99-0)
EPA Substance Registry System: benzyl 5-O-(2,3-dideoxy-α-DL-threo-hex-2-enopyranosyl)-2,3-O-isopropylidene-β-D-ribofuranoside(64035-99-0)

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: 64035-99-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 64035-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,3 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64035-99:
(7*6)+(6*4)+(5*0)+(4*3)+(3*5)+(2*9)+(1*9)=120
120 % 10 = 0
So 64035-99-0 is a valid CAS Registry Number.

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64035-99-0Relevant academic research and scientific papers

SYNTHESIS AND GLYCOSIDATION REACTIONS OF ACETYLATED RACEMIC PSEUDOGLYCALS

Angerbauer, Rolf,Schmidt, Richard R.

, p. 193 - 202 (2007/10/02)

The Diels-Alder reaction of 1,3-butadienylene diacetate with activated carbonyl compounds yields O-acetylated pseudoglycals (hex-2-enopyranoses).These reactive compounds are used for highly stereoselective syntheses of α-glycosides.Conformational analysis

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