Cas 1017587-22-2,(2R,3R,4R,5S)-(3,4-dibenzyloxy-N-tert-butoxycarbonyl-5-hydroxy-2-piperidinyl)methanol

1017587-22-2

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Basic information

Product Name: (2R,3R,4R,5S)-(3,4-dibenzyloxy-N-tert-butoxycarbonyl-5-hydroxy-2-piperidinyl)methanol
Synonyms: (2R,3R,4R,5S)-(3,4-dibenzyloxy-N-tert-butoxycarbonyl-5-hydroxy-2-piperidinyl)methanol
CAS NO:1017587-22-2
Molecular Formula:
Molecular Weight: 443.54
EINECS: N/A
Product Categories: N/A
Mol File: 1017587-22-2.mol
Article Data: 1

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: (2R,3R,4R,5S)-(3,4-dibenzyloxy-N-tert-butoxycarbonyl-5-hydroxy-2-piperidinyl)methanol(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4R,5S)-(3,4-dibenzyloxy-N-tert-butoxycarbonyl-5-hydroxy-2-piperidinyl)methanol(1017587-22-2)
EPA Substance Registry System: (2R,3R,4R,5S)-(3,4-dibenzyloxy-N-tert-butoxycarbonyl-5-hydroxy-2-piperidinyl)methanol(1017587-22-2)

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: 1017587-22-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1017587-22-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,7,5,8 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1017587-22:
(9*1)+(8*0)+(7*1)+(6*7)+(5*5)+(4*8)+(3*7)+(2*2)+(1*2)=142
142 % 10 = 2
So 1017587-22-2 is a valid CAS Registry Number.

1017587-22-2Upstream product

1017587-21-1 (2R,3R,4R,5S)-(3,4-dibenzyloxy-N-tert-butoxycarbonyl-5-methoxymethyloxy-2-piperidinyl)methanol

1017587-22-2Downstream Products

19130-96-2 1,5-dideoxy-1,5-imino-D-glucitol

1017587-22-2Relevant articles and documents

Palladium(II)-catalyzed cyclization of urethanes and its application to a total synthesis of 1-deoxynojirimycin

Yokoyama, Hajime,Kobayashi, Hisatake,Miyazawa, Masahiro,Yamaguchi, Seiji,Hirai, Yoshiro

, p. 283 - 292 (2008/09/17)

We have employed a palladium(II)-catalyzed cyclization of allylic alcohol as a key reaction to achieve a total synthesis of the azasugar 1-deoxynojirimycin from o-mannitol. This reaction should be useful for the stereoselective construction of natural poly-substituted piperidine derivatives.

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