18967-42-5 Usage
Uses
Used in Medical Applications:
3,4-Dichlorobenzyl isothiocyanate is used as a potential therapeutic agent for its anti-carcinogenic, anti-inflammatory, and immune-modulating properties. It is being explored for its ability to modulate various biological pathways and processes, which could lead to the development of new treatments for various diseases.
Used in Industrial Applications:
In the industrial sector, 3,4-dichlorobenzyl isothiocyanate is used as a raw material in the production of rubber and other polymers. Its chlorine and sulfur content contribute to the compound's versatility and potential for use in various manufacturing processes.
Used in Pharmaceutical Development:
3,4-Dichlorobenzyl isothiocyanate is used as a key component in the development of new pharmaceuticals. Its isothiocyanate group is known for its potential health benefits, and researchers are investigating its role in the creation of novel drug candidates that could address a range of medical conditions.
However, it is important to note that due to the potentially harmful effects of 3,4-dichlorobenzyl isothiocyanate, its use must be thoroughly tested and regulated to ensure safety and efficacy in all applications.
Check Digit Verification of cas no
The CAS Registry Mumber 18967-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,6 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18967-42:
(7*1)+(6*8)+(5*9)+(4*6)+(3*7)+(2*4)+(1*2)=155
155 % 10 = 5
So 18967-42-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H5Cl2NS/c9-7-2-1-6(3-8(7)10)4-11-5-12/h1-3H,4H2
18967-42-5Relevant academic research and scientific papers
Synthesis and Octopaminergic Agonist Activity of 2-(Substituted benzylamino)-2-thiazolines
Hirashima, Akinori,Yoshii, Yutaka,Eto, Morifusa
, p. 1062 - 1065 (2007/10/02)
2-(Substituted benzylamino)-2-thiazolines (SBAT) were synthesized by a hydrochloric acid-catalyzed cyclization of the corresponding thioureas, using a reaction of 2-methylthio-2-thiazoline with substituted benzylamines or by alkylating 2-amino-2-thiazoline. 2-(Alkylthio)-2-thiazolines were obtained by alkylating 2-mercaptothiazoline.Most of the SBAT compounds activated adenylate cyclase in homogenates of cockroach ventral nerve cords; the effect of introducing substituents at the phenyl of the SBAT compounds on octopaminergic agonist activity was not significant. 2--2-thiazolines and 2-(alkylthio)-2-thiazolines were not significant octopaminergic agonists.Washing removed nearly all of the activity of one of the SBAT compounds, suggesting that the SBAT compounds bound reversibly to the octopaminergic receptor.
