Cas 120966-34-9,2-[(3S,5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-Dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yloxy]-2-methyl-tetrahydro-pyran

120966-34-9

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Basic information

Product Name: 2-[(3S,5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-Dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yloxy]-2-methyl-tetrahydro-pyran
Synonyms:
CAS NO:120966-34-9
Molecular Formula:
Molecular Weight: 486.822
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: 2-[(3S,5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-Dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yloxy]-2-methyl-tetrahydro-pyran(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(3S,5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-Dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yloxy]-2-methyl-tetrahydro-pyran(120966-34-9)
EPA Substance Registry System: 2-[(3S,5S,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-Dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yloxy]-2-methyl-tetrahydro-pyran(120966-34-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 120966-34-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120966-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,6 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 120966-34:
(8*1)+(7*2)+(6*0)+(5*9)+(4*6)+(3*6)+(2*3)+(1*4)=119
119 % 10 = 9
So 120966-34-9 is a valid CAS Registry Number.

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120966-34-9Relevant academic research and scientific papers

Redox Glycosidation via Thionoester Intermediates

Barrett, Anthony G.M.,Bezuidenhoudt, Barend C.B.,Howell, Amy R.,Lee, Albert C.,Russell, Mark A.

, p. 2275 - 2277 (1989)

Several steroidal glycosides were prepared via esterification with aldonic acids, Lawesson thionation, lithium triethylborohydride mediated reductive methylation, and silver(I)-catalyzed ring closure.

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