6268-05-9

Basic information

• Product Name: CI 37155
• Synonyms: AZOIC DIAZO NO 24;CI 37155;FAST BLUE SALT RR;FAST BLUE RR;FAST BLUE RR BASE;LABOTEST-BB LT00133744;Azoic Diazo Component 24 (37155);FAST BLUE RR, 97% (C.I. 37155)
• CAS NO: 6268-05-9
• Molecular Formula: C₁₅H₁₆N₂O₃
• Molecular Weight: 272.3
• EINECS: 228-441-6
• Mol File: 6268-05-9.mol
• Article Data: 1

Chemical Properties

• Melting Point: 165-168 °C(lit.)
• Boiling Point: 378.2 °C at 760 mmHg
• Flash Point: 182.5 °C
• Appearance: purple-brown powder
• Density: 1.245 g/cm³
• Vapor Pressure: 6.38E-06mmHg at 25°C
• Refractive Index: 1.636
• Storage Temp.: 2-8°C
• PKA: 12.05±0.70(Predicted)
• CAS DataBase Reference: CI 37155(CAS DataBase Reference)
• NIST Chemistry Reference: CI 37155(6268-05-9)
• EPA Substance Registry System: CI 37155(6268-05-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 6268-05-9(Hazardous Substances Data)

Usage

Description

CI 37155, also known as N-(4-Amino-2,5-dimethoxyphenyl)benzamide, is a chemical compound that has been identified for its potential applications in various fields. It is characterized by its unique molecular structure, which includes an amide group and a substituted phenyl ring.

Uses

Used in Pharmaceutical Industry:
CI 37155 is used as a precursor in the preparation of Indazoles, which are a class of compounds known for their ability to inhibit one or more receptor or non-receptor tyrosine or serine/threonine kinases. These kinases play a crucial role in various cellular processes, including cell growth, differentiation, and apoptosis. By inhibiting these kinases, Indazoles can potentially be used in the development of therapeutic agents for the treatment of various diseases, such as cancer and inflammatory disorders.
In addition to its use in the pharmaceutical industry, CI 37155 may also have applications in other fields, such as materials science, where it could be used to develop new materials with unique properties. However, further research and development would be required to explore these potential applications fully.

InChI:InChI=1/C15H16N2O3/c1-19-13-9-12(14(20-2)8-11(13)16)17-15(18)10-6-4-3-5-7-10/h3-9H,16H2,1-2H3,(H,17,18)

Upstream product

• 135-45-5 N-(2,5-Dimethoxyphenyl)benzamide 
• 92-20-6 N-(2,5-Dimethoxy-4-nitrophenyl)benzamide 

Downstream Products

• 262436-51-1 N-[2,5-dimethoxy-4-(p-tolylsulfonylamino)phenyl]thiobenzamide 
• 1240915-28-9 4-methoxy-2,7-diphenyl[1,3]thiazolo[4,5-g][1,3]benzothiazole 
• 1240915-33-6 N-(5-methoxy-2-phenylbenzothiazol-6-yl)thiobenzamide 
• 1240915-22-3 N,N'-(2,5-dimethoxyphenyl)-1,4-dithiobenzamide 
• 151474-74-7 (5-Benzoylamino-4,7-dimethoxy-1-methyl-1H-indole-3-carbothioyl)-carbamic acid ethyl ester 
• 151474-77-0 2-(5-Benzoylamino-4,7-dimethoxy-1-methyl-1H-indol-3-yl)-thiazole-4-carboxylic acid amide 
• 151474-76-9 2-(5-Benzoylamino-1-methyl-4,7-dioxo-4,7-dihydro-1H-indol-3-yl)-thiazole-4-carboxylic acid amide 
• 151474-72-5 N-{4-[(2,2-Diethoxy-ethyl)-methyl-amino]-2,5-dimethoxy-phenyl}-benzamide 
• 151474-75-8 N-(4,7-Dimethoxy-1-methyl-3-thiocarbamoyl-1H-indol-5-yl)-benzamide 
• 151474-73-6 N-(4,7-Dimethoxy-1-methyl-1H-indol-5-yl)-benzamide 
• 595607-54-8 N-[4-(6-azido-hexanoylamino)-2,5-dimethoxy-phenyl]-benzamide 
• 595607-53-7 N-[4-(5-azido-pentanoylamino)-2,5-dimethoxy-phenyl]-benzamide 
• 595607-52-6 N-[4-(4-azido-butyrylamino)-2,5-dimethoxy-phenyl]-benzamide 
• 595607-51-5 N-[4-(3-azido-propionylamino)-2,5-dimethoxy-phenyl]-benzamide 

Relevant articles and documents

Reactions of some N-(2,5-dimethoxyaryl)thiobenzamides: En route to an analogue of kuanoniamine A

The reactions of some N-(2,5-dimethoxyaryl) thiobenzamides were studied. It was found that nitration of 2-aryl-4,7-dimethoxybenzothiazoles produced a mixture of 5- and 6-nitrobenzothiazoles which were distinguished by synthesis of the 2-aryl-4,7-dimethoxy-6-nitrobenzothiaoles by oxidative cyclization of the corresponding nitrothiobenzanilides. The results showed that the cyclization of arylthioanilides was influenced by the nature of the ring substituents.