Cas 128910-24-7,(3aR,3bS,6aR,7aR)-2,2-Dimethyl-tetrahydro-furo[2',3':4,5]furo[2,3-d][1,3]dioxole-5,6-dione 6-(O-benzyl-oxime)

128910-24-7

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Basic information

Product Name: (3aR,3bS,6aR,7aR)-2,2-Dimethyl-tetrahydro-furo[2',3':4,5]furo[2,3-d][1,3]dioxole-5,6-dione 6-(O-benzyl-oxime)
Synonyms: (3aR,3bS,6aR,7aR)-2,2-Dimethyl-tetrahydro-furo[2',3':4,5]furo[2,3-d][1,3]dioxole-5,6-dione 6-(O-benzyl-oxime)
CAS NO:128910-24-7
Molecular Formula:
Molecular Weight: 319.314
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: (3aR,3bS,6aR,7aR)-2,2-Dimethyl-tetrahydro-furo[2',3':4,5]furo[2,3-d][1,3]dioxole-5,6-dione 6-(O-benzyl-oxime)(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,3bS,6aR,7aR)-2,2-Dimethyl-tetrahydro-furo[2',3':4,5]furo[2,3-d][1,3]dioxole-5,6-dione 6-(O-benzyl-oxime)(128910-24-7)
EPA Substance Registry System: (3aR,3bS,6aR,7aR)-2,2-Dimethyl-tetrahydro-furo[2',3':4,5]furo[2,3-d][1,3]dioxole-5,6-dione 6-(O-benzyl-oxime)(128910-24-7)

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: 128910-24-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128910-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,9,1 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128910-24:
(8*1)+(7*2)+(6*8)+(5*9)+(4*1)+(3*0)+(2*2)+(1*4)=127
127 % 10 = 7
So 128910-24-7 is a valid CAS Registry Number.

128910-24-7Upstream product

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128910-24-7Relevant academic research and scientific papers

EFFICIENT SYNTHESIS OF (+)-NOJIRIMYCIN AND (+)-1-DEOXYNOJIRIMYCIN

Anzeveno, Peter B.,Creemer, Laura J.

, p. 2085 - 2088 (1990)

(+)-Nojirimycin (1a) and (+)-1-deoxynojirimycin (2) have been prepared from 1,2-O-isopropylidene-α-D-glucofuranurono-6,3-lactone (3) by a route involving stereoselective reductive amination of 5-hydroxy-1,2-O-isopropylidene-α-D-xylo-hexofuranurono-6,3-lactone (5a).

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