28266-87-7 Usage
Uses
Used in Pharmaceutical Industry:
4-AMINO-2-METHYL-BENZENEMETHANAMINE DIHYDROCHLORIDE is used as a precursor in the synthesis of various drugs, primarily for its role in creating anti-inflammatory and analgesic medications. Its ability to contribute to the development of therapeutic agents makes it a valuable component in the advancement of pharmaceutical formulations.
Used in Research and Development:
In the realm of research and development, 4-AMINO-2-METHYL-BENZENEMETHANAMINE DIHYDROCHLORIDE is employed as a key component in the exploration and creation of new drugs. Its unique properties allow researchers to investigate its potential applications and interactions within various chemical and biochemical processes, thereby aiding in the discovery of novel therapeutic agents.
Used in Chemical and Biochemical Research:
4-AMINO-2-METHYL-BENZENEMETHANAMINE DIHYDROCHLORIDE is utilized in chemical and biochemical research for its distinctive characteristics and potential use in drug development. Its involvement in these studies helps to broaden the understanding of its capabilities and to identify new avenues for its application in the creation of effective pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 28266-87-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,6 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28266-87:
(7*2)+(6*8)+(5*2)+(4*6)+(3*6)+(2*8)+(1*7)=137
137 % 10 = 7
So 28266-87-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2.2ClH/c1-6-4-8(10)3-2-7(6)5-9;;/h2-4H,5,9-10H2,1H3;2*1H
28266-87-7Relevant academic research and scientific papers
SYNTHESIS AND PROPERTIES OF 3- AND 4-AMINOBENZYLAMINE DERIVATIVES
Kraska, Jan,Teodorczyk, Zygmunt
, p. 1025 - 1034 (2007/10/02)
Derivatives of 3- and 4-aminobenzylamine substituted by chlorine atom, methyl or methoxyl group in the ring position 2, 4, 5 or 6 were synthesized.Structures of the compounds obtained were confirmed by spectroscopic (IR, NMR) and physico-chemical methods. pKa values were determined for the prepared amines and correlated with ? constants of substituents.The values of ?n meta and ?n para were found for the methylammonium group.
