Cas 445412-03-3,(3aS,6S,6aS)-6-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-4-one O-benzyl-oxime

445412-03-3

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Basic information

Product Name: (3aS,6S,6aS)-6-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-4-one O-benzyl-oxime
Synonyms: (3aS,6S,6aS)-6-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-4-one O-benzyl-oxime
CAS NO:445412-03-3
Molecular Formula:
Molecular Weight: 363.411
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: (3aS,6S,6aS)-6-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-4-one O-benzyl-oxime(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,6S,6aS)-6-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-4-one O-benzyl-oxime(445412-03-3)
EPA Substance Registry System: (3aS,6S,6aS)-6-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-4-one O-benzyl-oxime(445412-03-3)

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: 445412-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 445412-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,5,4,1 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 445412-03:
(8*4)+(7*4)+(6*5)+(5*4)+(4*1)+(3*2)+(2*0)+(1*3)=123
123 % 10 = 3
So 445412-03-3 is a valid CAS Registry Number.

445412-03-3Upstream product

445412-03-3Downstream Products

4099-88-1 2,3-O-isopropylidene-L-ribofuranose

445412-03-3Relevant academic research and scientific papers

Novel synthesis of L-ribose from D-mannono-1,4-lactone.

Takahashi, Hideyo,Iwai, Yoshinori,Hitomi, Yuko,Ikegami, Shiro

, p. 2401 - 2403 (2002)

[reaction: see text] D-Mannono-1,4-lactone was efficiently converted into L-ribose in eight steps. A key step of this synthesis is the cyclization of a gamma-hydroxyalkoxamate under Mitsunobu conditions. It is noteworthy that the O-alkylation product was

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