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(+)-4-[(E)-2-Hydroxyethylidene]-6,6-dimethyl-2-cyclohexene-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73891-29-9

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73891-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73891-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,9 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73891-29:
(7*7)+(6*3)+(5*8)+(4*9)+(3*1)+(2*2)+(1*9)=159
159 % 10 = 9
So 73891-29-9 is a valid CAS Registry Number.

73891-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2(E),4-ochtodien-1,6(R*)-diol

1.2 Other means of identification

Product number -
Other names (R)-4-[2-Hydroxy-eth-(E)-ylidene]-6,6-dimethyl-cyclohex-2-enol

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:73891-29-9 SDS

73891-29-9Relevant academic research and scientific papers

SYNTHESES OF MARINE OCHTODANE ANTIFEEDANTS VIA HYDROLYTIC DEHALOGENATION

Zegarski, Joseph,Howard, Bruce M.

, p. 1363 - 1366 (2007/10/02)

The syntheses of five naturally occurring antifeedants of the ochtodane ring system (1-ethyl-3,3-dimethylcyclohexane), previously isolated from the marine red alga Ochtodes crockeri, are reported.A key synthetic step involves the hydrolytic debromination of 6-bromo-1,4-ochtodien-3-ol.

NEW OCHTODANE SYNTHESES FROM MYRCENE

Masaki, Yukio,Hashimoto, Kinji,Sakuma, Kazuhiko,Kaji, Kenji

, p. 1481 - 1484 (2007/10/02)

The ochtodane skeleton is formed stereoselectively from myrcene via acid-catalyzed cyclization of the benzenesulfenyl chloride adduct and the epoxide in a biogenetic type fashion.Its application to the syntheses of two ochtodane-type monoterpenes, an aldehyde component of the boll weevil pheromone and a diol found in the red alga Ochtodes crockeri, is reported.

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