Cas 134209-35-1,(6E,10E)-(1R,3R,14S,15S,16S)-15-Benzyloxy-1,3,7,11-tetramethyl-17-oxa-tricyclo[12.3.0.0<sup>3,16</sup>]heptadeca-6,10-diene

134209-35-1

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Product Name: (6E,10E)-(1R,3R,14S,15S,16S)-15-Benzyloxy-1,3,7,11-tetramethyl-17-oxa-tricyclo[12.3.0.0^3,16]heptadeca-6,10-diene
Synonyms: (6E,10E)-(1R,3R,14S,15S,16S)-15-Benzyloxy-1,3,7,11-tetramethyl-17-oxa-tricyclo[12.3.0.0^3,16]heptadeca-6,10-diene
CAS NO:134209-35-1
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: (6E,10E)-(1R,3R,14S,15S,16S)-15-Benzyloxy-1,3,7,11-tetramethyl-17-oxa-tricyclo[12.3.0.0^3,16]heptadeca-6,10-diene(CAS DataBase Reference)
NIST Chemistry Reference: (6E,10E)-(1R,3R,14S,15S,16S)-15-Benzyloxy-1,3,7,11-tetramethyl-17-oxa-tricyclo[12.3.0.0^3,16]heptadeca-6,10-diene(134209-35-1)
EPA Substance Registry System: (6E,10E)-(1R,3R,14S,15S,16S)-15-Benzyloxy-1,3,7,11-tetramethyl-17-oxa-tricyclo[12.3.0.0^3,16]heptadeca-6,10-diene(134209-35-1)

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: 134209-35-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134209-35-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,2,0 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134209-35:
(8*1)+(7*3)+(6*4)+(5*2)+(4*0)+(3*9)+(2*3)+(1*5)=101
101 % 10 = 1
So 134209-35-1 is a valid CAS Registry Number.

134209-35-1Upstream 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

134209-35-1Downstream Products

134209-35-1Relevant academic research and scientific papers

Cyclization of Epoxyneocembrene Derivatives to Secotrinervitanes

Hirukawa, Toshifumi,Koarai, Akira,Kato, Tadahiro

, p. 4520 - 4525 (2007/10/02)

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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