99858-14-7 Usage
Uses
Used in Chemical Synthesis:
Butan-2-yl[(2,4-dichlorophenyl)methyl]amine is used as a reagent in the chemical synthesis industry for the preparation of secondary amines. It plays a crucial role in selective alkylation reactions involving primary amines and alkyl bromides, facilitating the formation of desired secondary amine products with precision and efficiency.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, butan-2-yl[(2,4-dichlorophenyl)methyl]amine may be utilized as an intermediate in the synthesis of various drug compounds. Its unique structure allows it to serve as a building block for the development of new medications, potentially contributing to the creation of novel therapeutic agents.
Used in Research and Development:
butan-2-yl[(2,4-dichlorophenyl)methyl]amine is also valuable in research and development settings, where it can be employed to study the effects of different chemical modifications on amine structures. Its use in these contexts can lead to a better understanding of chemical reactions and the properties of amines, ultimately contributing to advancements in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 99858-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,8,5 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 99858-14:
(7*9)+(6*9)+(5*8)+(4*5)+(3*8)+(2*1)+(1*4)=207
207 % 10 = 7
So 99858-14-7 is a valid CAS Registry Number.
99858-14-7Relevant academic research and scientific papers
Selective N-alkylation of primary amines with R-NH2·HBr and alkyl bromides using a competitive deprotonation/protonation strategy
Bhattacharyya, Shubhankar,Pathak, Uma,Mathur, Sweta,Vishnoi, Subodh,Jain, Rajeev
, p. 18229 - 18233 (2014/05/20)
Monoalkylation of primary amines using amine hydrobromides and alkyl bromides has been carried out. Under controlled reaction conditions the reactant primary amine was selectively deprotonated and made available for reaction, while the newly generated secondary amine remained protonated, and did not participate in alkylation further. Reaction was carried out under mild reaction conditions and was applicable to a wide range of primary amines and alkyl bromides.
