Cas 24165-34-2,(6E,10E)-(3aR,4R,11aR)-4-Hydroxy-3-methoxymethyl-6,10-dimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one

24165-34-2

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Basic information

Product Name: (6E,10E)-(3aR,4R,11aR)-4-Hydroxy-3-methoxymethyl-6,10-dimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one
Synonyms:
CAS NO:24165-34-2
Molecular Formula:
Molecular Weight: 280.364
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: (6E,10E)-(3aR,4R,11aR)-4-Hydroxy-3-methoxymethyl-6,10-dimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (6E,10E)-(3aR,4R,11aR)-4-Hydroxy-3-methoxymethyl-6,10-dimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one(24165-34-2)
EPA Substance Registry System: (6E,10E)-(3aR,4R,11aR)-4-Hydroxy-3-methoxymethyl-6,10-dimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one(24165-34-2)

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: 24165-34-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 24165-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,6 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24165-34:
(7*2)+(6*4)+(5*1)+(4*6)+(3*5)+(2*3)+(1*4)=92
92 % 10 = 2
So 24165-34-2 is a valid CAS Registry Number.

24165-34-2Upstream product

69859-90-1 C₁₉H₃₁NO₃

24165-34-2Downstream Products

24165-34-2Relevant academic research and scientific papers

DIETHYLAMINE ADDITION TO NATURAL SESQUITERPENIC α-EXOMETHYLENE-γ-LACTONES AND ITS USE FOR CHEMICAL TRANSFORMATIONS OF THESE COMPOUNDS

Harmatha, Juraj,Samek, Zdenek

, p. 2779 - 2785 (2007/10/02)

Addition of diethylamine to exomethylene double bond in natural sesquiterpenic α-methylene-γ-lactones is more advantageous in structural studies than the addition of other amines used so far.In some instances a simultaneous solvolysis of the ester groups also takes place.This fact was made use of for selective deacylation.The possibility of solvolysis impairs the potential use of diethylamine and other amines for the isolations of α-methylene-γ-lactone fractions directly from the extract of natural material.

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