56004-83-2 Usage
Description
2-(METHYLTHIO)BENZYLAMINE is a chemical compound that belongs to the group of aromatic amines. It is characterized by a benzene ring with a thiomethyl group attached to the benzyl carbon and an amine functional group. This versatile compound is known for its potential applications in various fields, including organic synthesis, chemical reactions, antimicrobial and antifungal properties, as well as in the pharmaceutical and agrochemical industries.
Uses
Used in Organic Synthesis:
2-(METHYLTHIO)BENZYLAMINE is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows it to be a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Reactions:
As a reagent, 2-(METHYLTHIO)BENZYLAMINE is utilized in a range of chemical reactions to facilitate the formation of desired products. Its presence can enhance reaction rates, improve yields, or enable specific reaction pathways.
Used in Pharmaceutical Industry:
2-(METHYLTHIO)BENZYLAMINE is used as a starting material or intermediate in the development of new pharmaceutical compounds. Its antimicrobial and antifungal properties make it a promising candidate for the treatment of various infections and diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(METHYLTHIO)BENZYLAMINE is employed for the development of new pesticides, herbicides, and fungicides. Its potential to combat microbial and fungal threats to crops makes it a valuable asset in agricultural research and product development.
Overall, 2-(METHYLTHIO)BENZYLAMINE is a multifaceted compound with a wide array of applications across different industries, making it an important entity in chemical and biological research.
Check Digit Verification of cas no
The CAS Registry Mumber 56004-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,0 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56004-83:
(7*5)+(6*6)+(5*0)+(4*0)+(3*4)+(2*8)+(1*3)=102
102 % 10 = 2
So 56004-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NS/c1-10-8-5-3-2-4-7(8)6-9/h2-5H,6,9H2,1H3
56004-83-2Relevant articles and documents
Steric hindrance effects in tripodal ligands for extraction and back-extraction of Ag+
Hiruta, Yuki,Watanabe, Takafumi,Nakamura, Etsuko,Iwasawa, Naoko,Sato, Hiroyasu,Hamada, Kensaku,Citterio, Daniel,Suzuki, Koji
, p. 9791 - 9798 (2014/03/21)
A novel series of tripodal ligands with thiophenylether arms connected to an anchoring nitrogen has been investigated. Seven tripodal ligands were synthesized by combining methyl, isopropyl, and tert-butyl residue bearing thiophenylether sites as groups w
N-Substituted aziridine-2-carboxylic acid derivatives for immuno stimulation
-
, (2008/06/13)
Aziridine-2-carboxylic acid derivatives of the formula STR1 wherein X is a carboxyl, nitrile, alkoxycarbonyl or carbamoyl group, and R and R1 are various organic radicals, or pharmacologically acceptable salts thereof, exhibit marked immunostimulant activity, especially in conjunction with added chemotherapeutic agents such as a penicillin, a cephalosporin, a nitrofuran or chloramphenicol. Those compounds are new where X is a cyano group or an alkoxycarbonyl radical and R1 is a hydrogen atom, but R' is not an unsubstituted alkyl radical or an alkyl radical substituted by hydroxyl, alkoxy, dialkylamino, phenyl, 4-chlorophenyl or 4-methoxyphenyl or a vinyl radical substituted by a phenyl or methyl radical, or a cycloalkyl radical, a phenyl a 4-chlorophenyl, a 4-methoxyphenyl, an s-triazinyl or a pyridinyl radical; or where X is a carbamoyl group and R1 is a hydrogen atom, R' is not an unsubstituted cyclohexyl, alkyl or benzyl radical; or where X is a cyano group or an alkoxycarbonyl radical and R1 is a phenyl radical, R' is not an isopropyl, cyclohexyl, phenyl, benzyl or p-chlorobenzyl radical; or where R1 is a methyl radical, R1 is not a benzyl, p-chloro- or p- methoxybenzyl radical.
