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

35879-90-4

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35879-90-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35879-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,7 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35879-90:
(7*3)+(6*5)+(5*8)+(4*7)+(3*9)+(2*9)+(1*0)=164
164 % 10 = 4
So 35879-90-4 is a valid CAS Registry Number.

35879-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name isokarahanaenone

1.2 Other means of identification

Product number -
Other names 1,5,5-Trimethyl-cyclohept-1-en-4-on

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:35879-90-4 SDS

35879-90-4Downstream Products

35879-90-4Relevant academic research and scientific papers

Acid-catalysed Rearrangement of Terpinolene Oxide

Gurudutt, K. N.,Pasha, M. A.,Ravindranath, B.

, p. 820 - 823 (2007/10/02)

The title reaction has been examined in detail and the effects of solvent and the acid catalyst on the nature of the products elucidated.Novel 1,3-dioxolanes, with potential use as aroma chemicals, have been prepared from terpinolene oxide (2) by an efficient method.

LEWIS ACID CATALYSED PINACOL REARRANGEMENT - A SHORT SYNTHESIS OF KARAHANAENONE

Bhushan, Vidya,Chandrasekaran, Srinivasan

, p. 1537 - 1538 (2007/10/02)

The pinacolic coupling reaction has been effectively used to prepare the unsymmetrical pinacol 2 and this key intermediate underwent a smooth ring enlargement to the monoterpene karahanaenone 3, an odoriferous constituent of Japanese hop and Cypress oil.

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