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3-Cyclohexen-1-ol, 4-(1,5-dimethyl-4-hexenyl)-1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139623-49-7

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139623-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139623-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,6,2 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 139623-49:
(8*1)+(7*3)+(6*9)+(5*6)+(4*2)+(3*3)+(2*4)+(1*9)=147
147 % 10 = 7
So 139623-49-7 is a valid CAS Registry Number.

139623-49-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,5-Dimethyl-4-hexenyl)-1-methyl-3-cyclohexen-1-ol

1.2 Other means of identification

Product number -
Other names Opt.-inakt. 1-Hydroxy-1-methyl-4-(1.5-dimethyl-hexen-(4)-yl)-cyclohexen-(3)

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:139623-49-7 SDS

139623-49-7Relevant academic research and scientific papers

Terpenes and Terpene Derivatives, XVIII. - Concerning the Preparation of rac-γ-Curcumene

Weyerstahl, Peter,Marschall-Weyerstahl, Helga,Scholz, Stefan

, p. 1021 - 1029 (2007/10/02)

Preparation of pure γ-curcumene (3) described by Birch in 1949 via dehydratization of the alcohol 5 with SOCl2/pyridine was not reproducible.Mixtures of α-, β-, and γ-curcumene (1-3) were obtained even with POCl3/pyridine or Burgess reagent.Analogously the secondary alcohol 20 yielded mixtures of 3 and the 1,3-dienes 21 and (presumably) 22. - Li/NH3 reduction of the tert. benzyl alcohol 8 afforded after work-up directly the dienone 15 which with MeLi gave the dehydro derivative 16 of zingiberenol (17).

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