Cas 1187972-08-2,tert-butyl (R)-4-[(1R,2S,3S)-1,2-bis(benzyloxy)-3,6-dihydroxyhexyl]-2,2-dimethyloxazolidine-3-carboxylate

1187972-08-2

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Basic information

Product Name: tert-butyl (R)-4-[(1R,2S,3S)-1,2-bis(benzyloxy)-3,6-dihydroxyhexyl]-2,2-dimethyloxazolidine-3-carboxylate
Synonyms: tert-butyl (R)-4-[(1R,2S,3S)-1,2-bis(benzyloxy)-3,6-dihydroxyhexyl]-2,2-dimethyloxazolidine-3-carboxylate
CAS NO:1187972-08-2
Molecular Formula:
Molecular Weight: 529.674
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: tert-butyl (R)-4-[(1R,2S,3S)-1,2-bis(benzyloxy)-3,6-dihydroxyhexyl]-2,2-dimethyloxazolidine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (R)-4-[(1R,2S,3S)-1,2-bis(benzyloxy)-3,6-dihydroxyhexyl]-2,2-dimethyloxazolidine-3-carboxylate(1187972-08-2)
EPA Substance Registry System: tert-butyl (R)-4-[(1R,2S,3S)-1,2-bis(benzyloxy)-3,6-dihydroxyhexyl]-2,2-dimethyloxazolidine-3-carboxylate(1187972-08-2)

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: 1187972-08-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1187972-08-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,7,9,7 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1187972-08:
(9*1)+(8*1)+(7*8)+(6*7)+(5*9)+(4*7)+(3*2)+(2*0)+(1*8)=202
202 % 10 = 2
So 1187972-08-2 is a valid CAS Registry Number.

1187972-08-2Upstream product

1187972-07-1 tert-butyl (R)-4-[(1R,2S,3S)-1,2-bis(benzyloxy)-6-hydroxy-3-(triethylsilyloxy)hexyl]-2,2-dimethyloxazolidine-3-carboxylate

1187972-08-2Downstream Products

1187972-08-2Relevant academic research and scientific papers

Stereoselective syntheses of the glycosidase inhibitors hyacinthacine A2, hyacinthacine A3 and 5-epi-hyacinthacine A3

Ribes, Celia,Falomir, Eva,Carda, Miguel,Marco, J. Alberto

experimental part, p. 6965 - 6971 (2009/12/06)

Stereoselective syntheses of the naturally occurring glycosidase inhibitors hyacinthacines A2 and A3 are reported. In the case of hyacinthacine A2, the pyrrolizidine system was created from an acyclic precursor via a doubl

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