Cas 359888-07-6,Benzoic acid (3S,5S,8R,9S,10S,14S,16S)-3-acetoxy-10,17-dimethyl-2,3,4,5,6,7,8,9,10,11,12,14,15,16-tetradecahydro-1H-cyclopenta[a]phenanthren-16-ylmethyl ester

359888-07-6

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Basic information

Product Name: Benzoic acid (3S,5S,8R,9S,10S,14S,16S)-3-acetoxy-10,17-dimethyl-2,3,4,5,6,7,8,9,10,11,12,14,15,16-tetradecahydro-1H-cyclopenta[a]phenanthren-16-ylmethyl ester
Synonyms:
CAS NO:359888-07-6
Molecular Formula:
Molecular Weight: 450.618
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: Benzoic acid (3S,5S,8R,9S,10S,14S,16S)-3-acetoxy-10,17-dimethyl-2,3,4,5,6,7,8,9,10,11,12,14,15,16-tetradecahydro-1H-cyclopenta[a]phenanthren-16-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (3S,5S,8R,9S,10S,14S,16S)-3-acetoxy-10,17-dimethyl-2,3,4,5,6,7,8,9,10,11,12,14,15,16-tetradecahydro-1H-cyclopenta[a]phenanthren-16-ylmethyl ester(359888-07-6)
EPA Substance Registry System: Benzoic acid (3S,5S,8R,9S,10S,14S,16S)-3-acetoxy-10,17-dimethyl-2,3,4,5,6,7,8,9,10,11,12,14,15,16-tetradecahydro-1H-cyclopenta[a]phenanthren-16-ylmethyl ester(359888-07-6)

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: 359888-07-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 359888-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,8,8 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 359888-07:
(8*3)+(7*5)+(6*9)+(5*8)+(4*8)+(3*8)+(2*0)+(1*7)=216
216 % 10 = 6
So 359888-07-6 is a valid CAS Registry Number.

359888-07-6Upstream product

359888-07-6Downstream Products

359888-07-6Relevant academic research and scientific papers

Neighboring group participation. Part 14. The preparation of the four stereoisomers of 16-hydroxymethyl-5α-androstane-3β,17-diol

Tapolcsanyi,Woelfling,Schneider

, p. 623 - 635 (2001)

16α-Hydroxymethyl-5α-androstane-3β,17β-diol and 16β-hydroxymethyl-5α-androstane-3β,17β-diol, were obtained from reduction of 16-acetoxymethylene-5α-androstan-17-one. The corresponding 16α,17α- and 16β,17α-hydroxymethyl isomers were obtained by neighboring group participation of the 16- and 17-acetates, respectively. The reactions involving carbocation formation also led to ring D rearrangement products. Copyright

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