4279-22-5 Usage
Uses
Used in Pharmaceutical Industry:
2,2-Dichlorobutane is used as a synthetic intermediate for the production of various pharmaceuticals. Its chemical properties make it suitable for the synthesis of a range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 2,2-Dichlorobutane serves as a precursor in the synthesis of agrochemicals. It aids in the creation of products designed to protect crops and enhance agricultural productivity, thereby supporting food security and crop yield.
Used in Polymer Industry:
2,2-Dichlorobutane is utilized as a component in the manufacture of polymers. Its role in polymer chemistry is vital for developing materials with specific properties required for various applications, including plastics, fibers, and coatings.
Used in Organic Compounds Synthesis:
Beyond its applications in specific industries, 2,2-Dichlorobutane is a versatile building block in the synthesis of a wide array of organic compounds. Its reactivity and stability make it an essential component in organic chemistry for creating new molecules with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4279-22-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4279-22:
(6*4)+(5*2)+(4*7)+(3*9)+(2*2)+(1*2)=95
95 % 10 = 5
So 4279-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H8Cl2/c1-3-4(2,5)6/h3H2,1-2H3
4279-22-5Relevant academic research and scientific papers
Surface-Catalyzed Reaction of the Gases Hydrogen Chloride and 2-Butyne
Mascavage, Linda M.,Zhang, Fan,Dalton, David R.
, p. 5048 - 5054 (2007/10/02)
Mixtures of gaseous hydrogen chloride and gaseous 2-butyne at total initial pressures less than 500 Torr, and at temperatures between 296 and 336 K, react in Pyrex IR cells (NaCl windows) to yield only (Z)-2-chloro-2-butene, i.e., the product of net trans (or anti or antarafacial) addition.Kinetic measurements have been made by observing the reaction throughout its course utilizing FT-IR spectroscopy.It is concluded that surface catalysis is required for product formation and that the reaction is occuring at the walls.
