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15733-63-8

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15733-63-8 Usage

Description

1-Chloro-5-phenylpentane, also known as 5-phenyl-1-chloropentane or pentane, 1-chloro-5-phenyl-, is an organic compound with the chemical formula C11H15Cl. It is an alkyl chloride, characterized by a chlorine atom attached to a carbon atom within a carbon chain. This colorless liquid exhibits a slightly sweet odor and is insoluble in water but soluble in many organic solvents. Due to its potential hazards to human health and the environment, it is crucial to handle this chemical with care and follow proper safety protocols.

Uses

Used in Pharmaceutical Industry:
1-Chloro-5-phenylpentane is used as an intermediate in the synthesis of various pharmaceuticals for its ability to facilitate the formation of new compounds through organic synthesis reactions.
Used in Agrochemical Industry:
1-Chloro-5-phenylpentane is used as a precursor in the production of agrochemicals, contributing to the development of new pesticides and other agricultural chemicals that enhance crop protection and yield.
Used in Organic Synthesis:
1-Chloro-5-phenylpentane is utilized as a reactant in organic synthesis processes, enabling the creation of a wide range of chemical compounds for various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 15733-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,3 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15733-63:
(7*1)+(6*5)+(5*7)+(4*3)+(3*3)+(2*6)+(1*3)=108
108 % 10 = 8
So 15733-63-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H15Cl/c12-10-6-2-5-9-11-7-3-1-4-8-11/h1,3-4,7-8H,2,5-6,9-10H2

15733-63-8 Well-known Company Product Price

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  • Alfa Aesar

  • (L08707)  1-Chloro-5-phenylpentane, 99%   

  • 15733-63-8

  • 1g

  • 1008.0CNY

  • Detail
  • Alfa Aesar

  • (L08707)  1-Chloro-5-phenylpentane, 99%   

  • 15733-63-8

  • 5g

  • 3967.0CNY

  • Detail

15733-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloropentylbenzene

1.2 Other means of identification

Product number -
Other names 5-Phenyl-1-pentyl chloride

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:15733-63-8 SDS

15733-63-8Relevant articles and documents

Catalytic remote hydrohalogenation of internal alkenes

Li, Xiang,Jin, Jianbo,Chen, Pinhong,Liu, Guosheng

, p. 425 - 432 (2022/02/07)

Primary alkyl halides have broad utility as fine chemicals in organic synthesis. The direct halogenation of alkenes is one of the most efficient approaches for the synthesis of these halides. Internal alkenes, in particular mixtures of isomers from refine

Catalytic Chemoselective and Stereoselective Semihydrogenation of Alkynes to E-Alkenes Using the Combination of Pd Catalyst and ZnI2

Maazaoui, Radhouan,Abderrahim, Raoudha,Chemla, Fabrice,Ferreira, Franck,Perez-Luna, Alejandro,Jackowski, Olivier

supporting information, p. 7544 - 7549 (2019/01/03)

An efficient E-selective semihydrogenation of internal alkynes was developed under low dihydrogen pressure and low reaction temperature from commercially available reagents: Cl2Pd(PPh3)2, Zn0, and ZnI2. Kinetic studies and control experiments underline the significant role of ZnI2 in this process under H2 atmosphere, establishing that the transformation involves syn-hydrogenation followed by isomerization. This simple and easy-to-handle system provides a route to E-alkenes under mild conditions.

Trichloroisocynuric acid/DMF as efficient reagent for chlorodehydration of alcohols under conventional and ultrasonic conditions

Venkana, Purugula,Kumar, Mukka Satish,Rajanna, Kamatala Chinna,Ali, Mir Moazzam

, p. 97 - 103 (2014/11/07)

A new and efficient method for the chlorodehydration of alcohols utilizing TCCA/DMF is described. Various alcohols can be converted smoothly into their corresponding alkyl chlorides in high yields under mild conditions with short reaction times. Taylor & Francis Group, LLC.

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