Cas 134237-93-7,(4E,8E)-(1R,12R,13S,14S)-14-Benzyloxy-4,8,12-trimethyl-15-methylene-bicyclo[10.2.2]hexadeca-4,8-dien-13-ol

134237-93-7

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Basic information

Product Name: (4E,8E)-(1R,12R,13S,14S)-14-Benzyloxy-4,8,12-trimethyl-15-methylene-bicyclo[10.2.2]hexadeca-4,8-dien-13-ol
Synonyms: (4E,8E)-(1R,12R,13S,14S)-14-Benzyloxy-4,8,12-trimethyl-15-methylene-bicyclo[10.2.2]hexadeca-4,8-dien-13-ol
CAS NO:134237-93-7
Molecular Formula:
Molecular Weight: 394.598
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: (4E,8E)-(1R,12R,13S,14S)-14-Benzyloxy-4,8,12-trimethyl-15-methylene-bicyclo[10.2.2]hexadeca-4,8-dien-13-ol(CAS DataBase Reference)
NIST Chemistry Reference: (4E,8E)-(1R,12R,13S,14S)-14-Benzyloxy-4,8,12-trimethyl-15-methylene-bicyclo[10.2.2]hexadeca-4,8-dien-13-ol(134237-93-7)
EPA Substance Registry System: (4E,8E)-(1R,12R,13S,14S)-14-Benzyloxy-4,8,12-trimethyl-15-methylene-bicyclo[10.2.2]hexadeca-4,8-dien-13-ol(134237-93-7)

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: 134237-93-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134237-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,2,3 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134237-93:
(8*1)+(7*3)+(6*4)+(5*2)+(4*3)+(3*7)+(2*9)+(1*3)=117
117 % 10 = 7
So 134237-93-7 is a valid CAS Registry Number.

134237-93-7Upstream product

134209-31-7 benzyl (1RS,2SR,3SR,6E,10E,14SR)-2,3-epoxy-14-(2-propenyl)-3,7,11-trimethyl-6,10-cyclotetradecadien-1-yl ether

134237-93-7Downstream Products

134237-93-7Relevant academic research and scientific papers

Cyclization of Epoxyneocembrene Derivatives to Secotrinervitanes

Hirukawa, Toshifumi,Koarai, Akira,Kato, Tadahiro

, p. 4520 - 4525 (1991)

Four stereoisomers of epoxyneocembrene derivatives 5-8 were treated with BF3*OEt2 as potential model reactions for the proposed biogenesis of secotrinervitane-type diterpenoids (Scheme I).Two of them (5 and 6) afforded secotrinervitane derivatives, while the remaining isomers 7 and 8 gave no cyclization products (Table I).The natural product, secotrinervitene-2β,3α-diol (2a) was synthesized from 5 in dl-form.

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