Cas 144102-24-9,2,2-Dimethyl-propionic acid (1S,3aS,7aS)-4-[(Z)-2-((S)-5-acetoxy-2-methyl-cyclohex-1-enyl)-vinyl]-7a-methyl-2,3,3a,6,7,7a-hexahydro-1H-inden-1-yl ester

144102-24-9

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Basic information

Product Name: 2,2-Dimethyl-propionic acid (1S,3aS,7aS)-4-[(Z)-2-((S)-5-acetoxy-2-methyl-cyclohex-1-enyl)-vinyl]-7a-methyl-2,3,3a,6,7,7a-hexahydro-1H-inden-1-yl ester
Synonyms:
CAS NO:144102-24-9
Molecular Formula:
Molecular Weight: 414.585
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: 2,2-Dimethyl-propionic acid (1S,3aS,7aS)-4-[(Z)-2-((S)-5-acetoxy-2-methyl-cyclohex-1-enyl)-vinyl]-7a-methyl-2,3,3a,6,7,7a-hexahydro-1H-inden-1-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,2-Dimethyl-propionic acid (1S,3aS,7aS)-4-[(Z)-2-((S)-5-acetoxy-2-methyl-cyclohex-1-enyl)-vinyl]-7a-methyl-2,3,3a,6,7,7a-hexahydro-1H-inden-1-yl ester(144102-24-9)
EPA Substance Registry System: 2,2-Dimethyl-propionic acid (1S,3aS,7aS)-4-[(Z)-2-((S)-5-acetoxy-2-methyl-cyclohex-1-enyl)-vinyl]-7a-methyl-2,3,3a,6,7,7a-hexahydro-1H-inden-1-yl ester(144102-24-9)

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: 144102-24-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 144102-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,1,0 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 144102-24:
(8*1)+(7*4)+(6*4)+(5*1)+(4*0)+(3*2)+(2*2)+(1*4)=79
79 % 10 = 9
So 144102-24-9 is a valid CAS Registry Number.

144102-24-9Upstream product

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144102-24-9Relevant academic research and scientific papers

PHOTOCHEMICAL AND THERMAL ISOMERIZATIONS OF C-19 FUNCTIONALIZED PREVITAMIN D ANALOGS IN THE ANDROSTANE SERIES

Sicinski, R. R.

, p. 191 - 200 (2007/10/02)

Upon irradiation of 3β-acetoxy-17β-trimethylacetoxy-5,7-androstadiene (1a) and its C-19-methyl, -acetoxy and -methoxy derivatives (1b, c, d), the corresponding androstane analogs of previtamin D and tachysterol (2 and 3) were formed.Thermal isomerization

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