10297-06-0 Usage
Description
6-CHLORO-1-HEXYNE is an organic compound characterized by its clear yellow liquid appearance. It is a chlorinated alkyne, which means it contains a chlorine atom and a carbon-carbon triple bond in its molecular structure. This unique composition endows 6-CHLORO-1-HEXYNE with specific chemical properties that make it suitable for various applications in different industries.
Uses
Used in Chemical Synthesis:
6-CHLORO-1-HEXYNE is used as an organic chemical synthesis intermediate for the production of various compounds. Its chemical properties, particularly the presence of the chlorine atom and the triple bond, make it a versatile building block in the synthesis of a wide range of organic molecules. The application reason is its ability to undergo various chemical reactions, such as substitution, addition, and elimination, which facilitate the formation of desired products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-CHLORO-1-HEXYNE is used as a key intermediate in the synthesis of certain pharmaceutical compounds. Its unique structural features allow it to be incorporated into drug molecules, potentially enhancing their biological activity and pharmacological properties. The application reason is its potential to contribute to the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
6-CHLORO-1-HEXYNE is also utilized in the agrochemical industry as an intermediate for the synthesis of various agrochemical products, such as pesticides and herbicides. Its chemical properties enable it to be transformed into active ingredients that can effectively control pests and weeds, thereby contributing to increased crop yields and improved agricultural productivity. The application reason is its role in the development of novel agrochemicals with enhanced performance and reduced environmental impact.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 6-CHLORO-1-HEXYNE is employed as an intermediate for the synthesis of various dyes and pigments. Its chemical structure allows it to be incorporated into dye molecules, potentially enhancing their color properties and stability. The application reason is its potential to contribute to the development of new dyes and pigments with improved performance characteristics, such as increased color strength, lightfastness, and resistance to fading.
Used in Polymer Industry:
6-CHLORO-1-HEXYNE is also used in the polymer industry as a monomer for the synthesis of specialty polymers. Its unique structural features can be exploited to create polymers with specific properties, such as improved mechanical strength, thermal stability, and chemical resistance. The application reason is its potential to contribute to the development of advanced polymer materials with a wide range of applications, including automotive, electronics, and packaging industries.
Check Digit Verification of cas no
The CAS Registry Mumber 10297-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,9 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10297-06:
(7*1)+(6*0)+(5*2)+(4*9)+(3*7)+(2*0)+(1*6)=80
80 % 10 = 0
So 10297-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H9Cl/c1-2-3-4-5-6-7/h1H,3-6H2
10297-06-0Relevant articles and documents
ω-alkyne-mono- and diphosphonates - Synthesis and sonogashira cross-coupling reaction with aryl halides
Delain-Bioton, Lise,Villemin, Didier,Jaffres, Paul-Alain
, p. 1274 - 1286 (2008/09/18)
A convergent approach to functionalise aromatic compounds with a linker terminated by a phosphonate group is reported. The starting point of this strategy is the synthesis of five new ω-alkyne-phosphonates. The linker between the phosphonate group and the alkyne part is either an alkyl or an ether chain. This strategy is based on the use of the phosphonate group as the anchoring point for the attachment of organic compounds onto alumina and the alkyne group, which is used to functionalise aryl halide compounds by a Sonogashira cross-coupling. The use of 1,10-phenanthroline as substrate illustrates the application of this strategy to an aromatic ligand. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.
Preparation of cycloalkylacetylene compounds using dialkylaminomagnesium halide or bis(dialkylamino)magnesium
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, (2008/06/13)
The process of invention reacts an alkynyl halide with a mixture that includes a dialkylaminomagnesium halide or a bis(dialkylamino)magnesium compound to produce a cycloalkylacetylene compound. Preferably, the dialkylaminomagnesium halide compound is of the general formula R 2 NMgX (where R is a linear, branched, or cyclic alkyl substituent or R 2 N represents a heterocyclic alkyl amine and X is Cl, Br, or I) and the bis(dialkylamino)magnesium compound is of the general formula (R 2 N) 2 Mg (where R is a linear, branched, or cyclic alkyl substituent or R 2 N represents a heterocyclic alkylamine). In a preferred method of the invention, the reaction is conducted at moderate temperatures for a period of about 12 to 24 hours. The reaction mixture preferably includes tetrahydrofuran (THF), or a hydrocarbon, or a hydrocarbonether mixture. The preferred compounds produced by this process are cycloalkylacetylene compounds having 5 to 20 carbons, such as cyclopropylacetylene and cyclobutylacetylene.
