Cas 129487-04-3,(1R,2R,4S,5R,6R,7S,10S)-12-Benzyl-4-methoxy-3,8,11-trioxa-12-aza-tricyclo[8.2.1.0<sup>2,7</sup>]tridecane-5,6-diol

129487-04-3

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Basic information

Product Name: (1R,2R,4S,5R,6R,7S,10S)-12-Benzyl-4-methoxy-3,8,11-trioxa-12-aza-tricyclo[8.2.1.0^2,7]tridecane-5,6-diol
Synonyms:
CAS NO:129487-04-3
Molecular Formula:
Molecular Weight: 337.373
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: (1R,2R,4S,5R,6R,7S,10S)-12-Benzyl-4-methoxy-3,8,11-trioxa-12-aza-tricyclo[8.2.1.0^2,7]tridecane-5,6-diol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,4S,5R,6R,7S,10S)-12-Benzyl-4-methoxy-3,8,11-trioxa-12-aza-tricyclo[8.2.1.0^2,7]tridecane-5,6-diol(129487-04-3)
EPA Substance Registry System: (1R,2R,4S,5R,6R,7S,10S)-12-Benzyl-4-methoxy-3,8,11-trioxa-12-aza-tricyclo[8.2.1.0^2,7]tridecane-5,6-diol(129487-04-3)

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: 129487-04-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129487-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,4,8 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 129487-04:
(8*1)+(7*2)+(6*9)+(5*4)+(4*8)+(3*7)+(2*0)+(1*4)=153
153 % 10 = 3
So 129487-04-3 is a valid CAS Registry Number.

129487-04-3Upstream product

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129487-04-3Relevant academic research and scientific papers

Intramolecular 1,3-dipolar additions in 4-O-allyl pyranoside 6-nitrones: An approach to chiral pyrano-pyrans and pyrano-oxepans

Collins,Ashwood,Eder,Wright,Kennedy

, p. 2055 - 2058 (1990)

Treatment of the easily prepared 6-aldehydo-glucopyranoside allyl ether (5) with N-benzylhydroxylarnine gave nitrone (6), which underwent a 1,3-dipolar addition to the 4-O-allyl group giving after deprotection and hydrogenolysis the chiral pyrano-pyran (1

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