Cas 83236-97-9,(R)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2,5-dimethoxy-2,5-dihydro-furan-2-yl)-methanol

83236-97-9

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Basic information

Product Name: (R)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2,5-dimethoxy-2,5-dihydro-furan-2-yl)-methanol
Synonyms: (R)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2,5-dimethoxy-2,5-dihydro-furan-2-yl)-methanol
CAS NO:83236-97-9
Molecular Formula:
Molecular Weight: 380.438
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: (R)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2,5-dimethoxy-2,5-dihydro-furan-2-yl)-methanol(CAS DataBase Reference)
NIST Chemistry Reference: (R)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2,5-dimethoxy-2,5-dihydro-furan-2-yl)-methanol(83236-97-9)
EPA Substance Registry System: (R)-((4S,5S)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2,5-dimethoxy-2,5-dihydro-furan-2-yl)-methanol(83236-97-9)

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: 83236-97-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 83236-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,2,3 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83236-97:
(7*8)+(6*3)+(5*2)+(4*3)+(3*6)+(2*9)+(1*7)=139
139 % 10 = 9
So 83236-97-9 is a valid CAS Registry Number.

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83236-97-9Relevant academic research and scientific papers

THE STEREOSELECTIVE SYNTHESIS OF L-TAGATOSE. AN APPLICATION OF Zn(II) MEDIATED HIGHLY STEREOSELECTIVE ADDITION OF 2-FURYLLITHIUM TO POLYOXYGENATED ALDEHYDE

Mukaiyama, Teruaki,Yuki, Yoichi,Suzuki, Keisuke

, p. 1169 - 1170 (2007/10/02)

In the presence of ZnBr2, the addition of 2-furyllithium to 4-O-benzyl-2,3-O-isopropylidene-L-threose proceeded in a highly stereoselective manner to afford the anti-adduct, which was further converted to L-tagatose.

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