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1,1-dimethyl-4-phenylbutyl chloride, also known as α,α-dimethyl-4-phenyl-1-butene chloride, is an organic compound with the chemical formula C12H17Cl. It is a colorless liquid with a molecular weight of 200.7 g/mol. 1,1-dimethyl-4-phenylbutyl chloride is characterized by its chlorinated butyl group attached to a phenyl ring, with two methyl groups on the first carbon. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity, it is essential to handle this chemical with care, as it can undergo various reactions such as nucleophilic substitution, elimination, and addition reactions.

4830-97-1

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4830-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4830-97-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4830-97:
(6*4)+(5*8)+(4*3)+(3*0)+(2*9)+(1*7)=101
101 % 10 = 1
So 4830-97-1 is a valid CAS Registry Number.

4830-97-1Relevant academic research and scientific papers

Isolable and Readily Handled Halophosphonium Pre-reagents for Hydro- and Deuteriohalogenation

Schevenels, Florian T.,Shen, Minxing,Snyder, Scott A.

supporting information, p. 6329 - 6337 (2017/09/12)

Although the addition of acid halides across olefins is well-studied, limitations remain with a number of substrate classes that possess leaving groups, polyunsaturation, and acid-sensitive moieties, particularly polyenes prone to cyclization. The process is also challenging when conducted on a small scale, and moreover, methods for the addition of their deuterated counterparts typically require special techniques, especially when control of stoichiometry is required. Herein is described a readily synthesized and handled reagent class which can accomplish the controlled and selective Markovnikov addition of both HCl and HBr across several alkene classes under mild reaction conditions tolerant of diverse functionality. The process is particularly valuable on a laboratory scale, and direct comparisons to other methods are provided. As a result of in-depth mechanistic studies seeking to understand how these novel tools work and the active species behind their efficacy, the means to easily add DCl and DBr using a controlled amount of D2O was discovered along with the critical role of hydrolysis in leading to active hydrohalogenation species.

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