29483-73-6

Basic information

• Product Name: 2-(2-AMINOPHENYL)BENZOTHIAZOLE 97
• Synonyms: 2-(2-AMINOPHENYL)BENZOTHIAZOLE 97;2-(benzo[d]thiazol-2-yl)aniline;2-(2-Aminophenyl)benzothiazole 97%
• CAS NO: 29483-73-6
• Molecular Formula: C₁₃H₁₀N₂S
• Molecular Weight: 226.302
• Product Categories: Building Blocks;Heterocyclic Building Blocks;Thiazoles
• Mol File: 29483-73-6.mol
• Article Data: 35

Chemical Properties

• Melting Point: 126-130 °C(lit.)
• Boiling Point: 417.8°C at 760 mmHg
• Flash Point: 206.5°C
• Appearance: /
• Density: 1.301g/cm³
• Vapor Pressure: 3.45E-07mmHg at 25°C
• Refractive Index: 1.73
• PKA: 1.13±0.10(Predicted)
• CAS DataBase Reference: 2-(2-AMINOPHENYL)BENZOTHIAZOLE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-AMINOPHENYL)BENZOTHIAZOLE 97(29483-73-6)
• EPA Substance Registry System: 2-(2-AMINOPHENYL)BENZOTHIAZOLE 97(29483-73-6)

Safety Data

• Hazard Codes: T
• Statements: 25-36/38
• Safety Statements: 26-36/37/39-45
• RIDADR: UN 2811 6.1/PG 3
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 29483-73-6(Hazardous Substances Data)

Usage

General Description

2-(2-aminophenyl)benzothiazole 97 is a chemical compound used in the manufacturing of various products such as dyes, pigments, and pharmaceuticals. It is a benzothiazole derivative that contains an aminophenyl group, making it suitable for use as a fluorescent dye. This chemical compound is also known for its potential applications in the field of organic electronics and optoelectronic devices. With a purity of 97%, it is considered as a high-quality material for research and industrial purposes. Additionally, it may also serve as a valuable intermediate in the synthesis of other functional organic compounds.

InChI:InChI=1/C13H10N2S/c14-10-6-2-1-5-9(10)13-15-11-7-3-4-8-12(11)16-13/h1-8H,14H2

Upstream product

• 118-48-9 isatoic anhydride 
• 137-07-5 2-amino-benzenethiol 
• 1843-21-6 N-phenyl-2-benzothiazolamine 
• 118-92-3 anthranilic acid 
• 60418-15-7 2-(2-Azidophenyl)benzothiazole 
• 6269-45-0 2-(2-nitrophenyl)benzo[d]thiazole 
• 615-43-0 2-iodophenylamine 
• 529-23-7 o-aminobenzaldehyde 
• 1141-88-4 2-Aminophenyl disulfide 
• 5344-90-1 2-Aminobenzyl alcohol 
• 555-16-8 4-nitrobenzaldehdye 
• 91-56-5 indole-2,3-dione 
• 2516-40-7 2-bromo-1,3-benzothiazole 
• 62-53-3 aniline 

Downstream Products

• 60418-15-7 2-(2-Azidophenyl)benzothiazole 
• 1161343-32-3 N-(2-(benzo[d]thiazol-2-yl)phenyl)-4'-chlorobiphenyl-4-sulfonamide 
• 1161343-30-1 N-(2-(benzo[d]thiazol-2-yl)phenyl)-4'-methoxybiphenyl-4-sulfonamide 
• 1092936-34-9 2-[2-(t-Boc-L-alanylamino)phenyl]benzothiazole 
• 1310352-08-9 2-[2-(t-Boc-β-alanylamino)phenyl]benzothiazole 
• 313665-69-9 C₂₀H₁₂ClN₃O₃S 
• 1395305-88-0 C₁₃H₁₁ClO₅*C₁₃H₁₀N₂S 
• 1616861-84-7 (2-(benzo[d]thiazole-2′-yl)-N-(but-2″-en-1″-yl)aniline) 
• 1508421-36-0 (2-(benzo[d]thiazole-2′-yl)-N-ethylaniline) 
• 1522132-66-6 (2-(benzo[d]thiazole-2′-yl)-N-isopropylaniline) 
• 1502486-47-6 (2-(benzo[d]thiazole-2′-yl)-N-butylaniline) 
• 1512093-30-9 (2-(benzo[d]thiazole-2′-yl)-N-propylaniline) 

Relevant articles and documents

Benzothiazole possessing reversible and reusable selective chemosensor for fluoride detection based on inhibition of excited state intramolecular proton transfer

A series of three benzothiazole derivatives BTBAs based on aryl amide groups have been developed, whose photophysical properties were remarkably changed by the presence of -OCH3and -NO2groups at para-position of aryl amides. Among th

Microwave-assisted neat synthesis of α-aminophosphonate/phosphinate derivatives of 2-(2-aminophenyl)benzothiazole as potent antimicrobial and antioxidant agents

A series of diethyl/ethylphenyl {2-(benzo[d]thiazol-2-yl)phenylamino}phosphonates and phosphinates were synthesized under microwave irradiation and neat conditions via Kabachnik-Fields reaction in high yields (80%–93%). The compounds were screened for antimicrobial and antioxidant properties. A few compounds showed effective antibacterial and antifungal activities at MIC value 12.5?μg/mL as compared with the standard at MIC value 6.25?μg/mL.

A new fluorescent probe for gasotransmitter H2S: High sensitivity, excellent selectivity, and a significant fluorescence off-on response

A fluorescent off-on probe for H2S was exploited by coupling the azide-based strategy with the excited-state intramolecular proton transfer (ESIPT) sensing mechanism, which exhibits a considerably high fluorescence enhancement (1150-fold), an e

Dual-Responsive Ratiometric Fluorescent Probe for Hypochlorite and Peroxynitrite Detection and Imaging In Vitro and In Vivo

Hypochlorite (ClO–) and peroxynitrite (ONOO–) are two crucial highly reactive oxygen/nitrogen species, which interplay with each other, and are implicated in numerous pathophysiological processes. The simultaneous detection of ClOsu

Construction and theoretical insights into the ESIPT fluorescent probe for imaging formaldehydein vitroandin vivo

We report the first ESIPT-based probeABTB, for the highly sensitive and selective imaging of formaldehyde (FA). The various theoretical calculations have been systematically performed, and clearly unravel the lighting mechanism of the fluorescent probe for FA. Additionally, the probe was successfully applied in monitoring endogenous FA in the brain of AD mice.

Selective Formation of 2-(2-Aminophenyl)benzothiazoles via Copper-Catalyzed Aerobic C?C Bond Cleavage of Isatins

Herein, two kinds of structurally significant 2-(2-aminophenyl)benzothiazoles were selectively generated by the copper-catalyzed aerobic C?C bond cleavage of isatins. Morpholine served not only as a reactant but a promoter in the three-component assembly of 2-(2-aminophenyl)benzothiazoles. Also it proved to be an efficient additive for the formation of free amino 2-(2-aminophenyl)benzothiazoles. This protocol represents a step-economic entry to the title compounds with a range of compatible functionalities. (Figure presented.).