Cas 960155-29-7,(3aR,4S,5R,6R,7S,7aR)-1-benzyl-4,6-bis(benzyloxy)-octahydrobenzo[c]isoxazole-5,7-diol

960155-29-7

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Basic information

Product Name: (3aR,4S,5R,6R,7S,7aR)-1-benzyl-4,6-bis(benzyloxy)-octahydrobenzo[c]isoxazole-5,7-diol
Synonyms: (3aR,4S,5R,6R,7S,7aR)-1-benzyl-4,6-bis(benzyloxy)-octahydrobenzo[c]isoxazole-5,7-diol
CAS NO:960155-29-7
Molecular Formula:
Molecular Weight: 461.558
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,4S,5R,6R,7S,7aR)-1-benzyl-4,6-bis(benzyloxy)-octahydrobenzo[c]isoxazole-5,7-diol(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,4S,5R,6R,7S,7aR)-1-benzyl-4,6-bis(benzyloxy)-octahydrobenzo[c]isoxazole-5,7-diol(960155-29-7)
EPA Substance Registry System: (3aR,4S,5R,6R,7S,7aR)-1-benzyl-4,6-bis(benzyloxy)-octahydrobenzo[c]isoxazole-5,7-diol(960155-29-7)

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: 960155-29-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 960155-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,1,5 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 960155-29:
(8*9)+(7*6)+(6*0)+(5*1)+(4*5)+(3*5)+(2*2)+(1*9)=167
167 % 10 = 7
So 960155-29-7 is a valid CAS Registry Number.

960155-29-7Upstream product

29601-98-7 N-benzylhydroxylamine hydrochloride

960155-29-7Downstream Products

960155-29-7Relevant academic research and scientific papers

Intra-molecular nitrone-olefin cycloaddition of d-glucose derived allylic alcohol: synthesis of new aminocyclohexitols

Chakraborty, Chaitali,Vyavahare, Vinod P.,Dhavale, Dilip D.

, p. 11984 - 11990 (2007)

Diastereo- and regioselelective intra-molecular nitrone-olefin cycloaddition reaction of in situ generated N-benzylnitrones, obtained from d-glucose derived precursors 5a/5b furnished dihydroxy functionalized isoxazolidines. The N-O bond reductive cleavag

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