Cas 138409-72-0,(R)-4-[(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-Pentamethyl-3-(2,2,2-trifluoro-acetoxy)-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-pentanoic acid

138409-72-0

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Basic information

Product Name: (R)-4-[(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-Pentamethyl-3-(2,2,2-trifluoro-acetoxy)-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-pentanoic acid
Synonyms:
CAS NO:138409-72-0
Molecular Formula:
Molecular Weight: 512.653
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: (R)-4-[(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-Pentamethyl-3-(2,2,2-trifluoro-acetoxy)-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-pentanoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (R)-4-[(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-Pentamethyl-3-(2,2,2-trifluoro-acetoxy)-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-pentanoic acid(138409-72-0)
EPA Substance Registry System: (R)-4-[(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-Pentamethyl-3-(2,2,2-trifluoro-acetoxy)-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-pentanoic acid(138409-72-0)

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: 138409-72-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138409-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 138409-72:
(8*1)+(7*3)+(6*8)+(5*4)+(4*0)+(3*9)+(2*7)+(1*2)=140
140 % 10 = 0
So 138409-72-0 is a valid CAS Registry Number.

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138409-72-0Relevant academic research and scientific papers

Synthesis, specificity, and antifungal activity of inhibitors of the Candida albicans Δ24-sterol methyltransferase

Ator, Mark A.,Schmidt, Stanley J.,Adams, Jerry L.,Dolle, Roland E.,Kruse, Lawrence I.,Frey, Carrie L.,Barone, Janice M.

, p. 100 - 106 (1992)

A series of side chain modified analogues of cholesterol and lanosterol (1-10) have been synthesized and evaluated as inhibitors of the Candida albicans Δ24-sterol methyltransferase. Two sterol substrate analogues 1 and 2 which contained a 24-t

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