2855-08-5 Usage
Description
1-Chloro-3,3-dimethylbutane, also known as tert-butyl chloride, is an organic compound with the chemical formula C5H11Cl. It is a colorless, flammable liquid with a chlorinated branched-chain structure. 1-CHLORO-3,3-DIMETHYLBUTANE is characterized by its reactivity and versatility in chemical reactions, making it a valuable component in various industrial applications.
Uses
1-Chloro-3,3-dimethylbutane is used as a raw material and intermediate for organic synthesis, pharmaceuticals, and agrochemicals due to its unique chemical properties and reactivity.
Used in Organic Synthesis:
1-Chloro-3,3-dimethylbutane is used as a building block in the synthesis of various organic compounds. Its chlorinated structure allows for a range of reactions, such as substitution, elimination, and addition, which can lead to the formation of a wide array of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-chloro-3,3-dimethylbutane is utilized as an intermediate in the production of various drugs and active pharmaceutical ingredients. Its ability to participate in different types of chemical reactions makes it a valuable component in the synthesis of complex molecular structures.
Used in Agrochemicals:
1-Chloro-3,3-dimethylbutane is also employed in the agrochemical industry as a starting material for the synthesis of various pesticides, herbicides, and other agricultural chemicals. Its reactivity and stability contribute to the development of effective and targeted products for crop protection and management.
Check Digit Verification of cas no
The CAS Registry Mumber 2855-08-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,5 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2855-08:
(6*2)+(5*8)+(4*5)+(3*5)+(2*0)+(1*8)=95
95 % 10 = 5
So 2855-08-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O/c1-8-3-4-9(2)11(7-8)12(13)10-5-6-10/h3-4,7,10H,5-6H2,1-2H3
2855-08-5Relevant articles and documents
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Whitmore,Bernstein,Mixon
, p. 2539 (1938)
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γ-Silyl-stabilized tertiary ions? Solvolysis of 4-(trimethylsilyl)-2-chloro-2-methylbutane
Tilley, Leon J.,Shiner Jr.
, p. 564 - 576 (2007/10/03)
Rate constant, isotope-effect, and product studies of the solvolysis of 4-(trimethylsilyl)-2-chloro-2-methylbutane, 11, and its carbon analog, 2-chloro-2,5,5-trimethylhexane, 10, in aqueous ethanol and aqueous 2,2,2-trifluoroethanol (TFE) indicate very little participation of the γ-silyl substituent. These results are in sharp contrast to earlier reports on secondary γ-silyl substituted systems, in which the back lobe of the silicon-carbon bond has been shown to overlap with the carbocation p-orbital to form a so-called 'percaudally' stabilized intermediate. While the solvolytic behaviors of 11 and 10 are nearly identical in ethanol, differences in the TFE lead to the conclusion that there is a minor amount of participation by the silyl substituent in that solvent. Interestingly, this observation lends credence to an earlier suggestion that TFE is better than ethanol at stabilizing more highly delocalized ions. Copyright
Evidence for Electron Transfer, Radical and Ionic Pathways in the Decomposition of Diacyl Peroxide
Lee, Sueg-Geun
, p. 1361 - 1372 (2007/10/02)
The thermal decomposition mechanism of 4,4-dimethylpentanoyl m-chlorobenzoyl peroxide and its α- and β-dideuteriated analogues is described.Product analyses and CIDNP studies suggest that all three pathways, electron transfer, radical and ionic, are operative in decomposition of these peroxides.Two pulsed-NMR techniques have been employed to eliminate distortions of CIDNP intensities arising from spin-lattice relaxation.These quantitative CIDNP studies have revealed an additional pure ionic pathway which competes with the radical pair electron transfer pathway to form rearranged reaction products.
