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1-Chloro-4-(penta-1,3-dien-1-yl)benzene is an organic compound with the molecular formula C12H13Cl. It is a derivative of benzene, where one hydrogen atom is replaced by a chlorine atom at the 1st position, and a penta-1,3-dien-1-yl group is attached at the 4th position. 1-chloro-4-(penta-1,3-dien-1-yl)benzene is characterized by its aromatic structure and the presence of a conjugated diene system in the side chain. It is a colorless liquid with a pungent odor and is soluble in organic solvents. Due to its chemical structure, it can undergo various reactions, such as electrophilic aromatic substitution and addition reactions involving the diene system. 1-chloro-4-(penta-1,3-dien-1-yl)benzene has potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.

3909-99-7

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3909-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3909-99-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,0 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3909-99:
(6*3)+(5*9)+(4*0)+(3*9)+(2*9)+(1*9)=117
117 % 10 = 7
So 3909-99-7 is a valid CAS Registry Number.

3909-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chlorophenyl)-1,3-pentadiene

1.2 Other means of identification

Product number -
Other names 1-(4-Chlorphenyl)-pentadien-1,3

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

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More Details:3909-99-7 SDS

3909-99-7Relevant academic research and scientific papers

METAL COMPLEXES IN ORGANIC SYNTHESIS. VIII. ALLYLIC ALCOHOLS AS STARTING MATERIALS IN PALLADIUM-CATALYZED WITTIG-TYPE OLEFINIZATIONS.

Moreno-Manas,Truis

, p. 2154 - 2158 (1983)

Allylic alcohols, aldehydes, and triphenylphosphine participate in a one-pot process catalyzed by palladium, which is formally equivalent to the Wittig olefinization. It can be applied to both aliphatic and aromatic aldehydes. The resulting olefins which appear as mixtures of stereoisomers were fully hydrogenated. Two different mechanisms can account for the observed results.

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