Cas 112239-50-6,(E)-(4R,6R)-4-Acetoxy-2-(4-methyl-pent-3-enyl)-6-p-tolyl-hept-2-enoic acid methyl ester

112239-50-6

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Basic information

Product Name: (E)-(4R,6R)-4-Acetoxy-2-(4-methyl-pent-3-enyl)-6-p-tolyl-hept-2-enoic acid methyl ester
Synonyms:
CAS NO:112239-50-6
Molecular Formula:
Molecular Weight: 372.505
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: (E)-(4R,6R)-4-Acetoxy-2-(4-methyl-pent-3-enyl)-6-p-tolyl-hept-2-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(4R,6R)-4-Acetoxy-2-(4-methyl-pent-3-enyl)-6-p-tolyl-hept-2-enoic acid methyl ester(112239-50-6)
EPA Substance Registry System: (E)-(4R,6R)-4-Acetoxy-2-(4-methyl-pent-3-enyl)-6-p-tolyl-hept-2-enoic acid methyl ester(112239-50-6)

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: 112239-50-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112239-50-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,3 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112239-50:
(8*1)+(7*1)+(6*2)+(5*2)+(4*3)+(3*9)+(2*5)+(1*0)=86
86 % 10 = 6
So 112239-50-6 is a valid CAS Registry Number.

112239-50-6Upstream product

112239-52-8 (E)-(4R,6R)-4-Acetoxy-6-((1R,4S)-4-hydroxy-4-methyl-cyclohex-2-enyl)-2-(4-methyl-pent-3-enyl)-hept-2-enoic acid methyl ester

112239-50-6Downstream Products

112239-50-6Relevant academic research and scientific papers

A NEW CLASS OF MONOCYCLIC DITERPENES FROM EREMOPHILA FOLIOSISSIMA KRAENZLIN. (MYOPORACEAE)

Forster, P. G.,Ghisalberti, E. L.,Jefferies, P. R.

, p. 2999 - 3008 (2007/10/02)

Three diterpene acids, representing a new class of monocyclic diterpenes, have been isolated from E. foliosissima Kraenzlin. (Myoporaceae).Chemical and spectroscopic evidence is presented for their stucture and absolute configuration.These diterpenes can

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