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Epiisocembrol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80126-41-6

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80126-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80126-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,2 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80126-41:
(7*8)+(6*0)+(5*1)+(4*2)+(3*6)+(2*4)+(1*1)=96
96 % 10 = 6
So 80126-41-6 is a valid CAS Registry Number.

80126-41-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2E,4S,7E,11E)-2,7,11-cembratrien-4-ol

1.2 Other means of identification

Product number -
Other names (2E,7E,11E)-(1S,4S)-4-Isopropyl-1,7,11-trimethyl-cyclotetradeca-2,7,11-trienol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:80126-41-6 SDS

80126-41-6Relevant academic research and scientific papers

PHOTOCHEMICAL ROUTE TO CEMBRANOIDS CONTAINING A cis-DISUBSTITUTED DOUBLE BOND

Vorob'ev, A. V.,Shevtsov, S. A.,Raldugin, V. A

, p. 150 - 156 (2007/10/02)

The 2-cis isomers of the natural diterpenoids isocembrol, 4-epiisocembrol, and isocembrene have been synthesized from a norcembrane ketone by the use of photochemical methods.

Decaryiol, a New Cembrane Diterpene from the Marine Soft Coral Sarcophyton decaryi

Carmely, Shmuel,Groweiss, Amiram,Kashman, Yoel

, p. 4279 - 4284 (2007/10/02)

The petroleum ether extract of the soft coral Sarcophyton decaryi yielded the cembrane-type diterpenes thunbergol (1), decaryiol (4), and 3,4-epoxynephthenol (13) in addition to nephthenol and trocheliophorol as reported previously.Compounds 4 and 13 are new and were characterized by spectral data, degradative studies by ozonolysis, and chemical transformations.Nephthenol reacts with tetrabromocyclohexadienone to give 11, the 3-bromo analogue of decaryiol.Compounds 4 and 11 rearrange to an enol ether (10), thereby proving the cembranoid structure of 4. 3,4-Epoxynephthenol (13), the second new cembranoid, is believed to be the biogenetic precursor of decaryiol (4), and, indeed, 13 could be transformed into 4 by acid catalysis.

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