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5-Phenyl-2-hexene is an organic compound with the molecular formula C12H16. It is a colorless liquid with a strong, aromatic odor. This chemical is characterized by a hexene backbone, which consists of a six-carbon chain with a double bond between the second and third carbon atoms, and a phenyl group attached to the fifth carbon. 5-Phenyl-2-hexene is used as a fragrance ingredient and a chemical intermediate in the synthesis of various compounds, such as pharmaceuticals and agrochemicals. It is also employed in the production of specialty polymers and resins. Due to its reactive nature, it is essential to handle 5-phenyl-2-hexene with care, following proper safety guidelines to minimize potential health and environmental risks.

5696-82-2

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5696-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5696-82-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,9 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5696-82:
(6*5)+(5*6)+(4*9)+(3*6)+(2*8)+(1*2)=132
132 % 10 = 2
So 5696-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C23H17BrN2O2/c1-28-16-12-10-15(11-13-16)22-14-18(17-6-2-4-8-20(17)25-22)23(27)26-21-9-5-3-7-19(21)24/h2-14H,1H3,(H,26,27)

5696-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-bromophenyl)-2-(4-methoxyphenyl)quinoline-4-carboxamide

1.2 Other means of identification

Product number -
Other names 5-phenylhexene-2

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:5696-82-2 SDS

5696-82-2Downstream Products

5696-82-2Relevant academic research and scientific papers

Palladium-catalyzed double-bond migration of unsaturated hydrocarbons accelerated by tantalum chloride

Murai, Masahito,Nishimura, Kengo,Takai, Kazuhiko

supporting information, p. 2769 - 2772 (2019/03/23)

The operationally simple palladium-catalyzed double-bond migration without heteroatom-containing coordinating functional groups is described. Addition of TaCl5 as a second catalyst greatly enhanced the migration efficiency to provide β-alkylsty

Process for producing alkenyl-substituted aromatic hydrocarbons

-

Page column 11, (2008/06/13)

There are provided a process for producing an alkenyl-substituted aromatic hydrocarbon by alkenylation of an alkyl-substituted aromatic hydrocarbon having a hydrogen atom at the α-position of a side chain thereof with a conjugated diene, using a catalyst obtained by the action of an alkali metal compound and an alkali metal or an alkali metal hydroxide on an metal oxide selected from alumina or hydrotalcite by heating in a specific temperature range; and a process for producing an alkenyl-substituted aromatic hydrocarbon, characterized in that the reaction is carried out in the presence of an alkylaminopyridine of formula (1): wherein R1is hydrogen or C1-C6lower alkyl, and R1is C1-C6lower alkyl, using as a catalyst, Na metal, K metal, or an alloy thereof, or a catalyst carrying any of them on an inorganic compound support, or a catalyst obtained by the action of an alkali metal compound and alkali metal or an alkali metal hydride on a metal oxide selected from alumina, alkaline earth metal oxides, hydrotalcite, silica-alumina, or zeolite by heating in a temperature range of 70° C. to 700° C.

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