1203-55-0

Basic information

• Product Name: NAPHTHO[2,1-D]THIAZOL-2-YLAMINE
• Synonyms: IFLAB-BB F1386-0396;NAPHTHO[2,1-D][1,3]THIAZOL-2-AMINE;NAPHTHO[2,1-D]THIAZOL-2-YLAMINE;Naphtho[2,1-d]thiazol-2-amine (9CI);Zinc00366319;naphtho[2,1-d][1,3]thiazol-2-amine(SALTDATA: FREE);naphtho[2,1-d]thiazol-2-amine
• CAS NO: 1203-55-0
• Molecular Formula: C₁₁H₈N₂S
• Molecular Weight: 200.26
• Product Categories: BENZOTHIAZOLE
• Mol File: 1203-55-0.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 417.1°Cat760mmHg
• Flash Point: 206.1°C
• Appearance: /
• Density: 1.403g/cm³
• Vapor Pressure: 3.63E-07mmHg at 25°C
• Refractive Index: 1.83
• CAS DataBase Reference: NAPHTHO[2,1-D]THIAZOL-2-YLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: NAPHTHO[2,1-D]THIAZOL-2-YLAMINE(1203-55-0)
• EPA Substance Registry System: NAPHTHO[2,1-D]THIAZOL-2-YLAMINE(1203-55-0)

Safety Data

• Hazard Codes: T
• Statements: 25
• Safety Statements: 45
• Hazardous Substances Data: 1203-55-0(Hazardous Substances Data)

Usage

Uses

Naphtho[2,1-d][1,3]thiazol-2-amine is used in preparation of Heteroaryl compounds useful for producing OLEDs.

InChI:InChI=1/C11H8N2S/c12-11-13-9-6-5-7-3-1-2-4-8(7)10(9)14-11/h1-6H,(H2,12,13)

Upstream product

• 17931-25-8 2-chloronaphtho<2,1-d>thiazole 
• 6395-99-9 naphtho[2,1-d]thiazol-2-yl-(triphenyl-λ⁵-phosphanylidene)-amine 
• 1147550-11-5 ammonium thiocyanate 
• 91-59-8 naphthalen-2-ylamine 
• 540-72-7 sodium thiocyanide 
• 530-93-8 1,2,3,4-tetrahydronaphthalen-2-one 
• 17356-08-0 thiourea 
• 2243-58-5 2-naphthylhydrazine hydrochloride 
• 1636-33-5 2-naphthyl isothiocyanate 
• 1166-32-1 N,N'-di(2-naphthyl)thiourea 
• 521980-39-2 1-methyl-3-phenyl-2,4-dioxo-1,2,3,4-tetrahydroquinolin-3-yl thiocyanate 
• 20191-75-7 1-bromo-2-naphthylamine 
• 14837-64-0 3-amino-3H-naphtho[2,1-d]thiazol-2-ylideneamine 
• 3394-04-5 naphthalen-2-yl-thiourea 

Downstream Products

• 26130-38-1 1-naphtho[2,1-d]thiazol-2-yl-3-phenyl-urea 
• 63751-40-6 8-benzylidene-naphtho[2,1-d]imidazo[2,1-b]thiazol-9-one 
• 63751-41-7 8-(4-hydroxy-benzylidene)-imidazo[2,1-b]naphtho[2,1-d]thiazol-9-one 
• 63751-43-9 8-(4-isopropyl-benzylidene)-naphtho[2,1-d]imidazo[2,1-b]thiazol-9-one 
• 63751-42-8 8-(2-methoxy-benzylidene)-imidazo[2,1-b]naphtho[2,1-d]thiazol-9-one 
• 53338-20-8 2-aminonaphthalene-1-thiol 
• 65323-42-4 9-(4-methoxy-phenyl)-naphtho[2,1-d]imidazo[2,1-b]thiazole 
• 56921-81-4 9-(4-ethoxy-phenyl)-naphtho[2,1-d]imidazo[2,1-b]thiazole 
• 54295-03-3 9-(4-bromo-phenyl)-imidazo[2,1-b]naphtho[2,1-d]thiazole 
• 54223-12-0 9-(4-chloro-phenyl)-imidazo[2,1-b]naphtho[2,1-d]thiazole 
• 54223-11-9 9-phenyl-imidazo[2,1-b]naphtho[2,1-d]thiazole 
• 63751-44-0 8-(4-nitro-benzylidene)-naphtho[2,1-d]imidazo[2,1-b]thiazol-9-one 
• 63751-45-1 8-(3-nitro-benzylidene)-naphtho[2,1-d]imidazo[2,1-b]thiazol-9-one 
• 63751-48-4 8-[1-(4-nitro-phenyl)-pyrrol-2-ylmethylene]-imidazo[2,1-b]naphtho[2,1-d]thiazol-9-one 

Relevant articles and documents

Visible-light-initiated malic acid-promoted cascade coupling/cyclization of aromatic amines and KSCN to 2-aminobenzothiazoles without photocatalyst

By using ambient air as the oxidant and malic acid as the promoter, a practical method for the preparation of 2-aminobenzothiazoles through visible-light-initiated cascade reaction of aromatic amines and KSCN in eco-friendly bis(methoxypropy)ether under metal-, hazardous additive-, photocatalyst-free conditions was established.

NAPHTHO[2,1 -D]THIAZOLE DERIVATIVES, COMPOSITIONS THEREOF AND METHODS OF TREATING DISORDERS

The present application relates to the compounds of formula (I) that inhibit CDK9, pharmaceutical compositions thereof and methods of making and using the same.

Metal-free synthesis of 2-aminobenzothiazoles via aerobic oxidative cyclization/dehydrogenation of cyclohexanones and thioureas

A metal-free process for the synthesis of 2-aminobenzothiazoles from cyclohexanones and thioureas has been developed using catalytic iodine and molecular oxygen as the oxidant under mild conditions. Various 2-aminobenzothiazoles, 2-aminonaphtho[2,1-d]thiazoles, and 2-aminonaphtho[1,2-d] thiazoles were prepared via this method in satisfactory yields.