Cas 56845-81-9,Acetic acid (3S,10R,13R)-17-((1R,5S)-6-hydroxy-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

56845-81-9

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Basic information

Product Name: Acetic acid (3S,10R,13R)-17-((1R,5S)-6-hydroxy-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester
Synonyms:
CAS NO:56845-81-9
Molecular Formula:
Molecular Weight: 444.698
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: Acetic acid (3S,10R,13R)-17-((1R,5S)-6-hydroxy-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (3S,10R,13R)-17-((1R,5S)-6-hydroxy-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(56845-81-9)
EPA Substance Registry System: Acetic acid (3S,10R,13R)-17-((1R,5S)-6-hydroxy-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(56845-81-9)

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: 56845-81-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 56845-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,4 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56845-81:
(7*5)+(6*6)+(5*8)+(4*4)+(3*5)+(2*8)+(1*1)=159
159 % 10 = 9
So 56845-81-9 is a valid CAS Registry Number.

56845-81-9Upstream product

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56845-81-9Relevant academic research and scientific papers

On the C-25 Chirality of 26-Hydroxycholesterol

Byon, Chang-Yon,Gut, Marcel,Toome, Voldemar

, p. 3901 - 3903 (2007/10/02)

The stereospecific synthesis of (25S)-26-hydroxycholesterol with a chiral synthon derived from (S)-(+)-3-hydroxy-2-methylpropanoic acid is described and the Cotton effects of the CD spectra were found not to be a general means for distinguishing epimers of monohydric secondary alcohols or for distinguishing epimers in which the chiral center is in the α position to the primary alcoholic function.

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