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17699-05-7

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17699-05-7 Usage

General Description

2,6-dimethyl-6-(4-methyl-3-pentenyl)bicyclo[3.1.1]hept-2-ene is a chemical compound with a complex structure that contains two methyl groups and a pentenyl group attached to a bicyclic carbon framework. It is a bicyclic hydrocarbon with a molecular formula C14H22. This chemical is known for its unique structure and its potential applications in the field of organic chemistry. It is important to handle this chemical with care due to its complex structure and potential reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 17699-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,9 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17699-05:
(7*1)+(6*7)+(5*6)+(4*9)+(3*9)+(2*0)+(1*5)=147
147 % 10 = 7
So 17699-05-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H24/c1-11(2)6-5-9-15(4)13-8-7-12(3)14(15)10-13/h6-7,13-14H,5,8-10H2,1-4H3/t13-,14-,15-/m0/s1

17699-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name α-bergamotene

1.2 Other means of identification

Product number -
Other names Bicyclo[3.1.1]hept-2-ene, 2,6-dimethyl-6-(4-methyl-3-pentenyl)-

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:17699-05-7 SDS

17699-05-7Downstream Products

17699-05-7Relevant articles and documents

Isotope sensitive branching and kinetic isotope effects to analyse multiproduct terpenoid synthases from Zea mays

Gatto, Nathalie,Vattekkatte, Abith,K?llner, Tobias,Degenhardt, J?rg,Gershenzon, Jonathan,Boland, Wilhelm

supporting information, p. 3797 - 3800 (2015/03/30)

Multiproduct terpene synthases TPS4-B73 and TPS5-Delprim from Zea mays exhibit isotopically sensitive branching in the formation of mono- and sesquiterpene volatiles. The impact of the kinetic isotope effects and the stabilization of the reactive intermediates by hyperconjugation along with the shift of products from alkenes to alcohols are discussed.

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