2809-65-6

Basic information

• Product Name: BENZENE,1-CHLORO-4-(1-PROPY
• Synonyms: BENZENE,1-CHLORO-4-(1-PROPY;1-(1-Propynyl)-4-chlorobenzene;1-(4-Chlorophenyl)-1-propyne;1-Chloro-4-(1-propynyl)benzene;Benzene, 1-chloro-4-(1-propyn-1-yl)-
• CAS NO: 2809-65-6
• Molecular Formula: C₉H₇Cl
• Molecular Weight: 150.6
• Mol File: 2809-65-6.mol
• Article Data: 23

Chemical Properties

• Boiling Point: 90 °C(Press: 10 Torr)
• Appearance: /
• Density: 1.12±0.1 g/cm3(Predicted)
• CAS DataBase Reference: BENZENE,1-CHLORO-4-(1-PROPY(CAS DataBase Reference)
• NIST Chemistry Reference: BENZENE,1-CHLORO-4-(1-PROPY(2809-65-6)
• EPA Substance Registry System: BENZENE,1-CHLORO-4-(1-PROPY(2809-65-6)

Safety Data

• Hazardous Substances Data: 2809-65-6(Hazardous Substances Data)

Usage

General Description

Benzene,1-chloro-4-(1-propyl) is a chemical compound with the molecular formula C9H11Cl. It is a chlorinated derivative of benzene and contains a propyl group attached to the fourth carbon atom. BENZENE,1-CHLORO-4-(1-PROPY is used in organic synthesis and manufacturing processes to produce a variety of products, including pharmaceuticals, pesticides, and dyes. It is also used as a solvent and a chemical intermediate in the production of other compounds. Benzene,1-chloro-4-(1-propyl) is considered to be a hazardous chemical and should be handled and stored with caution due to its potential health and environmental risks.

Upstream product

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• 70090-69-6 1-chloro-4-(prop-2-yn-1-yl)benzene 
• 5586-88-9 1-(4-chlorophenyl)propan-2-one 
• 66343-90-6 1-p-Chlorphenyl-aceton-tosylhydrazon 
• 5633-34-1 (benzoylmethylene)dimethylsulfurane 

Downstream Products

• 18826-55-6 2-p-Chlorphenyl-3-methyl-2-cyclopropen-1-carbonsaeure 
• 69645-14-3 2-p-Chlorphenyl-3-methyl-2-cyclopropen-1-carbonsaeuremethylester 
• 19824-38-5 ethylene glycol mono(4'-chlorobenzoate) 
• 1588773-66-3 (E)-2-(1-(4-chlorophenyl)prop-1-en-2-yl)-N,N-dimethyl-1H-indole-1-carboxamide 
• 1588773-26-5 2-(4-chlorophenyl)-1-methyl-3H-pyrrolo[1,2-a]indol-3-one 
• 1009-14-9 phenyl butyl ketone 
• 99-91-2 para-chloroacetophenone 
• 1820-42-4 bis(4-chlorophenyl)acetylene 
• 1380169-53-8 2,3,6-trimethyl-4-(4-chlorophenyl)pyridine 
• 1380169-60-7 2,4,6-trimethyl-3-(4-chlorophenyl)pyridine 
• 1380502-92-0 C₂₁H₁₆ClN₃ 

Relevant articles and documents

Copper-Catalyzed Synthesis of Tetrasubstituted Alkenes via Regio- and anti-Selective Addition of Silylboronates to Internal Alkynes

As a new and complementary method for the synthesis of structurally defined tetrasubstituted alkenes, a copper-catalyzed regio- and anti-selective addition of silylboronates to unsymmetric internal alkynes has been developed. A variety of unactivated alky

Regio- And stereoselective electrochemical synthesis of sulfonylated enethers from alkynes and sulfonyl hydrazides

An electrooxidative direct difunctionalization of internal alkynes with sulfonyl hydrazides has been developed for the construction of sulfonated enethers. In this transformation, metal catalysts or stoichiometric amount of oxidants are not required and molecular nitrogen and hydrogen are the sole byproducts, providing a simple and green approach for preparing various sulfonyl tetrasubstituted alkenes. Notably, the protocol could be efficiently scaled up and the follow-up procedures of the corresponding functionalized alkenes demonstrate the practicality of the electrochemical synthesis.

Palladium-catalyzed methylation of terminal alkynes

In this communication, a palladium-catalyzed procedure for the methylation of terminal alkynes has been developed. With N,N,N-trimethylbenzenaminium trifluoromethanesulfonate as the methyl source, various desired products were obtained in moderate to good yields. Both aromatic and aliphatic alkynes are applicable.