Cas 3827-30-3,(1R)-7α-Ethyl-1,2,3,4,4a,4bα,5,6,7,8,10,10aα-dodecahydro-1,4aβ,7-trimethyl-1α-phenanthrenecarboxylic acid methyl ester

3827-30-3

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Basic information

Product Name: (1R)-7α-Ethyl-1,2,3,4,4a,4bα,5,6,7,8,10,10aα-dodecahydro-1,4aβ,7-trimethyl-1α-phenanthrenecarboxylic acid methyl ester
Synonyms: (1R)-7α-Ethyl-1,2,3,4,4a,4bα,5,6,7,8,10,10aα-dodecahydro-1,4aβ,7-trimethyl-1α-phenanthrenecarboxylic acid methyl ester
CAS NO:3827-30-3
Molecular Formula: C21H34O2
Molecular Weight: 318.49346
EINECS: N/A
Product Categories: N/A
Mol File: 3827-30-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1R)-7α-Ethyl-1,2,3,4,4a,4bα,5,6,7,8,10,10aα-dodecahydro-1,4aβ,7-trimethyl-1α-phenanthrenecarboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1R)-7α-Ethyl-1,2,3,4,4a,4bα,5,6,7,8,10,10aα-dodecahydro-1,4aβ,7-trimethyl-1α-phenanthrenecarboxylic acid methyl ester(3827-30-3)
EPA Substance Registry System: (1R)-7α-Ethyl-1,2,3,4,4a,4bα,5,6,7,8,10,10aα-dodecahydro-1,4aβ,7-trimethyl-1α-phenanthrenecarboxylic acid methyl ester(3827-30-3)

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: 3827-30-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 3827-30-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,2 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3827-30:
(6*3)+(5*8)+(4*2)+(3*7)+(2*3)+(1*0)=93
93 % 10 = 3
So 3827-30-3 is a valid CAS Registry Number.

3827-30-3Upstream product

1686-62-0 isopimaric acid methyl ester

3827-30-3Downstream Products

3827-30-3Relevant academic research and scientific papers

β-Stereospecific Hydroboration of 13-epi-Pimar-8(14)-enes

Feliciano, Arturo San,Medarde, Manuel,Caballero, Esther,Tome, Fernando,Hebrero, Belen

, p. 1665 - 1670 (2007/10/02)

β-Stereospecific hydroborations of the Δ8(14)-double bond in 13-epi-pimarenes were achieved in the absence of functional groups at C-16 or a double bond at C-15.The reaction carried out on 15,16-dihydrosandaracopimaric derivatives needed more time and a large excess of reagent due to stereochemical restrictions in the transition state.

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