Cas 444910-33-2,(3aR,5S,6R,6aR)-5-Azidomethyl-6-(2-benzyloxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole

444910-33-2

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Basic information

Product Name: (3aR,5S,6R,6aR)-5-Azidomethyl-6-(2-benzyloxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole
Synonyms: (3aR,5S,6R,6aR)-5-Azidomethyl-6-(2-benzyloxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole
CAS NO:444910-33-2
Molecular Formula:
Molecular Weight: 333.387
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,5S,6R,6aR)-5-Azidomethyl-6-(2-benzyloxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,5S,6R,6aR)-5-Azidomethyl-6-(2-benzyloxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole(444910-33-2)
EPA Substance Registry System: (3aR,5S,6R,6aR)-5-Azidomethyl-6-(2-benzyloxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole(444910-33-2)

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: 444910-33-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 444910-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,9,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 444910-33:
(8*4)+(7*4)+(6*4)+(5*9)+(4*1)+(3*0)+(2*3)+(1*3)=142
142 % 10 = 2
So 444910-33-2 is a valid CAS Registry Number.

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444910-33-2Relevant academic research and scientific papers

1-Aza-sugars from D-Glucose. Preparation of 1-Deoxy-5-dehydroxymethyl-Nojirimycin, its analogues and evaluation of glycosidase inhibitory activity

Patil, Nitin T.,John, Sheeja,Sabharwal, Sushma G.,Dhavale, Dilip D.

, p. 2155 - 2160 (2007/10/03)

D-Glucose derived pentodialdoses 11a-c on reduction followed by tosylation, azide displacement, hydrogenation and protection with -Cbz group gave N-Cbz protected compounds 14a-c, respectively, which on removal of 1,2-acetonide functionality and hydrogenat

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