115398-34-0

Basic information

• Product Name: 4-AMINO-5-CHLORO-1,2,3-BENZOTHIADIAZOLE
• Synonyms: ASISCHEM C75326;AKOS BB-7861;5-CHLORO-BENZO[1,2,5]THIADIAZOL-4-YLAMINE;5 CHLORO 4 AMINO-2,1,3,BENZOTHIADIAZOLE;5-CHLORO-2,1,3-BENZOTHIADIAZOL-4-AMINE;4-AMINO-5-CHLORO-1,2,3-BENZOTHIADIAZOLE;4-AMINO-5-CHLOROPIAZTHIOLE;5-Chloro 2,1,3 Benzothidiazole 4 Amine
• CAS NO: 115398-34-0
• Molecular Formula: C6H4ClN3S
• Molecular Weight: 185.63
• Mol File: 115398-34-0.mol

Chemical Properties

• Melting Point: 89°C
• Appearance: /
• Refractive Index: 1.782
• CAS DataBase Reference: 4-AMINO-5-CHLORO-1,2,3-BENZOTHIADIAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINO-5-CHLORO-1,2,3-BENZOTHIADIAZOLE(115398-34-0)
• EPA Substance Registry System: 4-AMINO-5-CHLORO-1,2,3-BENZOTHIADIAZOLE(115398-34-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38-36
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 115398-34-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Electronics and Optoelectronics:
4-AMINO-5-CHLORO-1,2,3-BENZOTHIADIAZOLE is used as a key component in the development of organic electronic and optoelectronic devices due to its strong electron-accepting ability and high thermal stability. These properties contribute to the enhancement of device performance and reliability.
Used as a Pharmaceutical Intermediate:
In the pharmaceutical industry, 4-AMINO-5-CHLORO-1,2,3-BENZOTHIADIAZOLE serves as an intermediate in the synthesis of biologically active compounds. Its unique chemical structure allows for the creation of new drugs with potential therapeutic applications.
Used in Sensor Development:
4-AMINO-5-CHLORO-1,2,3-BENZOTHIADIAZOLE is utilized as a building block for the development of sensor materials. Its electron-accepting properties and thermal stability make it suitable for the creation of sensors with improved sensitivity and durability.
Used in Photovoltaic Devices:
In the field of photovoltaics, 4-AMINO-5-CHLORO-1,2,3-BENZOTHIADIAZOLE is employed as a component in the design of photovoltaic devices. Its unique properties contribute to the development of more efficient and stable solar cells and other related technologies.

InChI:InChI=1/C6H4ClN3S/c7-3-1-2-4-6(5(3)8)9-10-11-4/h1-2H,8H2

Upstream product

• 2274-89-7 5-chloro-4-nito-2,1,3-benzothiadiazole 
• 2207-32-1 5-chloro-2,1,3-benzothiadiazole 

Downstream Products

• 16407-86-6 5,7-Dichlor-4-amino-benz<2,1,3>-thiadiazol 
• 51322-75-9 tizanidine 
• 91982-37-5 7-hydrazino-thiazolo[4',5':3,4]benzo[1,2-c][1,2,5]thiadiazole 
• 173532-15-5 5-chloro-N-(N-acetyl-4,5-dihydro-1H-imidazol-2-yl)-2,1,3-benzothiadiazol-4-amine 
• 106314-85-6 tizanidine 2-hydroxypropionic acid salt 
• 64461-82-1 tizanidine hydrochloride 

Relevant articles and documents

COVALENT INHIBITORS OF KRAS G12C

Irreversible inhibitors of G12C mutant K-Ras protein are provided. Also disclosed are methods to modulate the activity of G12C mutant K-Ras protein and methods of treatment of disorders mediated by G12C mutant K-Ras protein.