Cas 96235-18-6,Acetic acid 2-[3-[3-(2-furan-3-yl-ethyl)-2-methyl-oxiranyl]-prop-(Z)-ylidene]-6-methyl-hept-5-enyl ester

96235-18-6

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Basic information

Product Name: Acetic acid 2-[3-[3-(2-furan-3-yl-ethyl)-2-methyl-oxiranyl]-prop-(Z)-ylidene]-6-methyl-hept-5-enyl ester
Synonyms:
CAS NO:96235-18-6
Molecular Formula:
Molecular Weight: 360.494
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: Acetic acid 2-[3-[3-(2-furan-3-yl-ethyl)-2-methyl-oxiranyl]-prop-(Z)-ylidene]-6-methyl-hept-5-enyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid 2-[3-[3-(2-furan-3-yl-ethyl)-2-methyl-oxiranyl]-prop-(Z)-ylidene]-6-methyl-hept-5-enyl ester(96235-18-6)
EPA Substance Registry System: Acetic acid 2-[3-[3-(2-furan-3-yl-ethyl)-2-methyl-oxiranyl]-prop-(Z)-ylidene]-6-methyl-hept-5-enyl ester(96235-18-6)

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: 96235-18-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96235-18-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,3 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96235-18:
(7*9)+(6*6)+(5*2)+(4*3)+(3*5)+(2*1)+(1*8)=146
146 % 10 = 6
So 96235-18-6 is a valid CAS Registry Number.

96235-18-6Upstream product

91176-46-4 Acetic acid (2Z,6E)-9-furan-3-yl-6-methyl-2-(4-methyl-pent-3-enyl)-nona-2,6-dienyl ester

96235-18-6Downstream Products

96235-18-6Relevant academic research and scientific papers

POLYENE CYCLIZATION : CYCLIZATION STUDIES ON AN ACYCLIC FURANODITERPENE AND ITS EPOXIDE

Pandey, U. C.,Sarmah, P.,Sharma, R. P.

, p. 3739 - 3748 (1984)

Reaction of an acyclic diterpene alcohol 1c with chlorotrimethylsilane and sodium iodide or SnCl4 furnishes compounds 7 and 8.This cyclization is reminiscent of the biosynthesis of pallescensins E-G - an analogous compounds in sesquiterpenoids.Reaction of the epoxide 2 with SnCl4 furnishes only the acyclic compounds 12, 13, 14a, 14c and 15a.Photolysis of 2 results in the formation of ( 4+2) photocycloaduct 21.

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