38254-49-8 Usage
Description
BroMo-tert-butyl Alcohol, also known as Bromo-tert-butyl Alcohol, is an organic compound characterized by its bromine atom and tert-butyl group. It is a versatile organic building block with a wide range of applications in various chemical synthesis processes due to its unique structural properties.
Uses
Used in Chemical Synthesis:
BroMo-tert-butyl Alcohol is used as an organic building block for the synthesis of various compounds, particularly in the production of Monohalogeno-t-butyloxycarbonylamino Acids. Its unique structure allows for the creation of a diverse array of molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, BroMo-tert-butyl Alcohol is utilized as a key intermediate in the synthesis of various drugs and drug candidates. Its ability to form stable bonds with other molecules makes it a valuable component in the development of new medications.
Used in Material Science:
BroMo-tert-butyl Alcohol is also employed in the field of material science, where it is used to create novel materials with specific properties. Its versatility in chemical reactions enables the development of materials with tailored characteristics for various applications, such as in coatings, adhesives, and polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 38254-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,5 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38254-49:
(7*3)+(6*8)+(5*2)+(4*5)+(3*4)+(2*4)+(1*9)=128
128 % 10 = 8
So 38254-49-8 is a valid CAS Registry Number.
38254-49-8Relevant articles and documents
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Huston,Brault
, p. 1211,1213,1215 (1950)
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Solvent Effects on the Rate of Heterolysis of t-Butyl Chloride, Bromide, Iodide, and 2,4-Dinitrophenolate
Mitsuhashi, Tsutomu,Hirota, Hiroshi,Yamamoto, Gaku
, p. 824 - 830 (2007/10/02)
Rates of heterolytic decompositions of t-butyl chloride, bromide, iodide, and 2,4-dinitrophenolate have been measured by an NMR method in eight deuterated or undeuterated polar solvents; methanol-d4, ethanol-d6, dimethyl-d6 sulfoxide, N,N-dimethylformamide-d7, acetonitrile-d3, pyridine, nitrobenzene, and acetone-d6.The observed solvent effect is discussed on the basis of cation and anion solvation.With t-butyl halides, the anion solvation due to hydrogen bonding by protic solvents drastically decreases on increasing the radius of halide ions, and thus the differential solvation transferred from anion-solvating methanol to cation-solvating dimethyl sulfoxide is dramatically reversed on going from the chloride to the iodide (kMe2SO-d6/kmethanol-d4 at 60 deg C: t-BuCl, 5E-2; t-BuBr, 6E-1; t-BuI, 7).The 2,4-dinitrophenolate behaves like the iodide.Complicated products are obtained in the decomposition of t-butyl bromide in dimethyl sulfoxide; however, a mechanism involving a bimolecular decomposition process of the bromide is ruled out.During the decomposition od t-butyl iodide in dimethyl sulfoxide, an intermediate salt t-butoxydimethylsulfonium iodide has been detected.The salt decomposes to isobutene, but the process is much slower than the heterolytic decomposition of t-butyl iodide itself at ambient temperature.
