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(E)-2,6,6-Trimethyl-α-(1-propenyl)-1-cyclohexene-1-methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35122-36-2

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35122-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35122-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,2 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35122-36:
(7*3)+(6*5)+(5*1)+(4*2)+(3*2)+(2*3)+(1*6)=82
82 % 10 = 2
So 35122-36-2 is a valid CAS Registry Number.

35122-36-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2,6,6-Trimethyl-α-(1-propenyl)-1-cyclohexene-1-methanol

1.2 Other means of identification

Product number -
Other names trans-2,6,6-trimethyl-1-[1-hydroxy-2-butenyl]-1-cyclohexene

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:35122-36-2 SDS

35122-36-2Relevant academic research and scientific papers

Allylsilanes derived from α- and β-ionone. Synthesis and unusual reactivity with electrophiles

Azzari,Faggi,Gelsomini,Taddei

, p. 6067 - 6070 (2007/10/02)

Silylcupration of α- and β-ionol acetates selectively gave the corresponding allylsilanes with direct substitution of the acetate with a trimethylsilyl group. Reactions of these products with electrophiles showed the unusual absence of the allylic shift, typical in nucleophilic condensations of allylsilanes. Ionotrimethylsilanes are effective building blocks for synthesis of terpenes and carotenoids.

Alkenoyl-cyclohexadienes

-

, (2008/06/13)

New cycloaliphatic unsaturated ketones and their use as perfuming and odour-modifying agents in the manufacture of perfumes and perfumed products, and as flavouring and taste-modifying agents in the preparation of foodstuffs in general and imitation flavours for foodstuffs, beverages, animal feeds, pharmaceutical preparations and tobacco products. Methods for the preparation of said cycloaliphatic unsaturated ketones.

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