81142-32-7 Usage
General Description
4-(Bromomethyl)-2,6-di-tert-butylpyridine is a chemical compound with the molecular formula C15H22BrN. It is a brominated pyridine derivative with two tert-butyl groups attached to the pyridine ring. 4-(BROMOMETHYL)-2,6-DI-TERT-BUTYLPYRIDINE is commonly used in organic synthesis and pharmaceutical research as a building block for the preparation of various biologically active compounds. It is also used as a starting material for the synthesis of complex molecules and for the modification of natural products. Additionally, it has potential applications in the field of materials science, such as in the development of new polymers and functional materials. As a bromine-containing compound, it is important to handle it with care and adhere to proper safety protocols when working with it.
Check Digit Verification of cas no
The CAS Registry Mumber 81142-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,4 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81142-32:
(7*8)+(6*1)+(5*1)+(4*4)+(3*2)+(2*3)+(1*2)=97
97 % 10 = 7
So 81142-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H22BrN/c1-13(2,3)11-7-10(9-15)8-12(16-11)14(4,5)6/h7-8H,9H2,1-6H3
81142-32-7Relevant articles and documents
Reactions of 2,6-Di-tert-butylpyridine Derivatives with Methyl Fluorosulfate under High Pressure
Hou, C. J.,Okamato, Yoshiyuki
, p. 1977 - 1979 (1982)
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SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF NUCLEASES
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Page/Page column 14;, (2019/11/12)
The invention provides compounds represented by the structural formula (1): wherein R1, R2, R3, R4, R5, R6 are as defined in the claims. The compounds are inhibitors of nucleases, and are useful in particular in a method of treatment and/or prevention of proliferative diseases, neurodegenerative diseases, and other genomic instability associated diseases.
Synthesis of some fluorinated pyridines using tetrabutylammonium fluoride
Mobinikhaledi,Foroughifar
, p. 405 - 412 (2007/10/03)
Some bromo- and chloromethyl pyridines were synthesized using radical substitution reactions. Further reaction of these halopyridines with activated tetrabutylammonium fluoride under mild conditions gave the related fluorinated pyridines. The yields of products following recrystallization were of the order of 30-93%. 1H, 13C, and 19F spectroscopies together with elemental analysis were used characterize products. Copyright Taylor & Francis Group, LLC.
