677304-89-1

Basic information

• Product Name: 7-Benzothiazolecarboxylicacid,2-amino-,ethylester(9CI)
• Synonyms: 7-Benzothiazolecarboxylicacid,2-amino-,ethylester(9CI);Ethyl 2-aMinobenzo[d]thiazole-7-carboxylate
• CAS NO: 677304-89-1
• Molecular Formula: C₁₀H₁₀N₂O₂S
• Molecular Weight: 222.26
• Product Categories: BENZOTHIAZOLE
• Mol File: 677304-89-1.mol

Chemical Properties

• Boiling Point: 386.789°C at 760 mmHg
• Flash Point: 187.724°C
• Appearance: /
• Density: 1.364g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.675
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: 7-Benzothiazolecarboxylicacid,2-amino-,ethylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Benzothiazolecarboxylicacid,2-amino-,ethylester(9CI)(677304-89-1)
• EPA Substance Registry System: 7-Benzothiazolecarboxylicacid,2-amino-,ethylester(9CI)(677304-89-1)

Safety Data

• Hazardous Substances Data: 677304-89-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
7-Benzothiazolecarboxylic acid, 2-amino-, ethyl ester (9CI) is used as a building block for the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 7-Benzothiazolecarboxylic acid, 2-amino-, ethyl ester (9CI) serves as a versatile intermediate for the preparation of a wide range of organic compounds. Its reactivity and functional groups enable chemists to synthesize complex molecules with specific properties and applications.

InChI:InChI=1/C10H10N2O2S/c1-2-14-9(13)6-4-3-5-7-8(6)15-10(11)12-7/h3-5H,2H2,1H3,(H2,11,12)

Upstream product

• 20967-87-7 3-[(aminothioxomethyl)amino]benzoic acid ethyl ester 
• 582-33-2 3-aminobenzoic acid ethyl ester 
• 677304-86-8 ethyl 2-amino-1,3-benzothiazole-7-carboxylate hydrobromide 
• 19045-66-0 thiocarbamic acid 

Downstream Products

• 677304-90-4 ethyl 1,3-benzothiazole-7-carboxylate 
• 99584-89-1 2-amino-benzothiazole-7-carboxylic acid hydrazide 
• 71224-95-8 2-aminobenzo[d]thiazole-7-carboxylic acid 

Relevant articles and documents

HETEROCYCLE-SUBSTITUTED BICYCLIC AZOLE PESTICIDES

Disclosed are compounds of Formula (I), including all geometric and stereoisomers, N-oxides, and salts thereof, Formula (I) wherein Q is Formula (I) and A, R1, m, X1, X2, X3, X4, Y1, Y

HETEROCYCLE-SUBSTITUTED BICYCLIC AZOLE PESTICIDES

Disclosed are compounds of Formula 1, including all geometric and stereoisomers, N-oxides, and salts thereof, and A, R1, m, X1, X2, X3, X4, Y1, Y2 and Y3 are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound or a composition of the invention.

INDAZOLES, BENZOTHIAZOLES, BENZOISOTHIAZOLES, BENZISOXAZOLES, AND PREPARATION AND USES THEREOF

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nACh receptors), activation of nACh receptors, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (e.g., indazoles and benzothiazoles), which act as ligands for the α7 nACh receptor subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

INDAZOLES, BENZOTHIAZOLES, AND BENZOISOTHIAZOLES, AND PREPARATION AND USES THEREOF

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nAChR), activation of nAChRs, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (indazoles and benzothiazoles), which act as ligands for the α7 nAChR subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.