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2-Penten-1-ol,3-methyl-5-(2,6,6-trimethyl-1-cyclohexen-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15353-35-2

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15353-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15353-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,5 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15353-35:
(7*1)+(6*5)+(5*3)+(4*5)+(3*3)+(2*3)+(1*5)=92
92 % 10 = 2
So 15353-35-2 is a valid CAS Registry Number.

15353-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name β-monocyclofarnesol

1.2 Other means of identification

Product number -
Other names -

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:15353-35-2 SDS

15353-35-2Downstream Products

15353-35-2Relevant academic research and scientific papers

FUNCTIONALISATION OF 1,3-ALPHA-DIENES (I)

-

Page/Page column 17, (2021/07/02)

The present invention relates to the functionalisation of specific 1,3-alpha-dienes. These functionalized 1,3-alpha-dienes are important intermediates in organic synthe- sis (especially in the synthesis of carotenoids, vitamin A and/or vitamin A derivatives).

Synthesis of tricyclic ketones with sesquiterpene skeletons by acid- catalyzed rearrangement of β-monocyclofarnesol

Frater, Georg,Mueller, Urs,Kraft, Philip

, p. 522 - 530 (2007/10/03)

Starting from dihydro-β-ionone (6) a mixture of three tricyclic ketones with sesquiterpene skeletons 14,15, and 16 was prepared by Wittig-Horner reaction with triethyl phosphonoacetate, Red-Al reduction, acid-catalyzed rearrangement of the resulting β-mon

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