2-Aminobenzothiazole-6-carboxylic acid
Uses- Product Name
- 2-Aminobenzothiazole-6-carboxylic acid
- CAS No.
- 93-85-6
- Chemical Name
- 2-Aminobenzothiazole-6-carboxylic acid
- Synonyms
- AKOS BB-7723;ASISCHEM B67429;AKOS BBS-00000327;SALOR-INT L481106-1EA;2-Aminobenzothiazolepurum;forspectrophotometricdet.(ofPd);2-Aminobenzothiazol-6-carbonsure;forgravimetricdetermination(ofHg);2-AMINO-6-BENZOTHIAZOLECARBOXYLIC ACID;2-AMINO-BENZOTHIAZOLE-6-CARBOXYLIC ACID
- CBNumber
- CB3780886
- Molecular Formula
- C8H6N2O2S
- Formula Weight
- 194.21
- MOL File
- 93-85-6.mol
2-Aminobenzothiazole-6-carboxylic acid Property
- Melting point:
- 265 ºC (DEC.)
- Boiling point:
- 466.6±37.0 °C(Predicted)
- Density
- 1.604
- storage temp.
- 2-8°C(protect from light)
- form
- solid
- pka
- 3.99±0.30(Predicted)
- color
- Off-white
- CAS DataBase Reference
- 93-85-6(CAS DataBase Reference)
- EPA Substance Registry System
- 6-Benzothiazolecarboxylic acid, 2-amino- (93-85-6)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405Store locked up.
N-Bromosuccinimide Price
- Product number
- L481106
- Product name
- 2-AMINO-1,3-BENZOTHIAZOLE-6-CARBOXYLIC ACID
- Purity
- Aldrich<sup>CPR</sup>
- Packaging
- 1 unit
- Price
- $185
- Updated
- 2025/07/31
- Product number
- L481106
- Product name
- 2-AMINO-1,3-BENZOTHIAZOLE-6-CARBOXYLIC ACID
- Purity
- Aldrich
- Packaging
- 250mg
- Price
- $179
- Updated
- 2024/03/01
- Product number
- A595883
- Product name
- 2-AMINO-1,3-BENZOTHIAZOLE-6-CARBOXYLIC ACID
- Packaging
- 10g
- Price
- $110
- Updated
- 2021/12/16
- Product number
- J51220
- Product name
- 2-Aminobenzo[d]thiazole-6-carboxylicacid
- Packaging
- 25g
- Price
- $110
- Updated
- 2021/12/16
- Product number
- 027026
- Product name
- 2-Amino-1,3-benzothiazole-6-carboxylic acid
- Purity
- 95%
- Packaging
- 25g
- Price
- $114
- Updated
- 2021/12/16
2-Aminobenzothiazole-6-carboxylic acid Chemical Properties,Usage,Production
Uses
2-Aminobenzothiazole-6-carboxylic acid is a heterocyclic organic compound that can be used as an organic intermediate. 2-Aminobenzothiazoles belong to a class of heterocyclic compounds with diverse biological activities. For example, riluzole, clinically used to treat amyotrophic lateral sclerosis (ALS), belongs to the 2-aminobenzothiazole class; fulenteazole has antiviral, anthelmintic, and immunosuppressive activities; N-acyl-substituted 2-aminobenzothiazoles can inhibit HIV; and N-aryl-substituted 2-aminobenzothiazoles have strong anticancer activity. 2-Aminobenzothiazoles are also widely used in the development of antibacterial, antiviral, and anti-inflammatory drugs for the treatment of Parkinson's disease and diabetes. Therefore, 2-aminobenzothiazoles occupy a very important position in medicinal chemistry.
Chemical Properties
Light brown powder
Antimicrobial activity
2-Aminobenzothiazole-6-carboxylic acid is a synthetic antibacterial agent that inhibits bacterial growth by binding to the enzyme urokinase-type plasminogen (uPA) and preventing it from converting plasminogen to plasmin. This drug has been shown to have inhibitory properties against a wide range of bacteria, including Staphylococcus and Escherichia coli.
Synthesis
540-72-7
150-13-0
93-85-6
Steps for the synthesis of 2-aminobenzothiazole-6-carboxylic acid: (2) Sodium thiocyanate (NaSCN, 65 g, 0.8 mol) was added to a methanol (MeOH) suspension of 4-aminobenzoic acid (1,100 g, 0.73 mol), followed by batch addition of bromine (Br2, 38 mL, 0.73 mol). The reaction mixture was cooled to -10 °C and stirred for 2 hours while keeping the internal temperature below -5 °C. Upon completion of the reaction, the precipitate was collected by filtration and suspended in 350 ml of 1 M hydrochloric acid (HCl). The suspension was heated to reflux and maintained for 30 minutes. After rapid filtration, 150 ml of concentrated hydrochloric acid (HCl) was added to the hot filtrate to give 70 g (42% yield) of 2-aminobenzothiazole-6-carboxylic acid (white solid). The product was dried and used directly without further purification.
References
[1] Patent: US2009/123373, 2009, A1. Location in patent: Page/Page column 14-15
2-Aminobenzothiazole-6-carboxylic acid Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 2-Aminobenzothiazole-6-carboxylic acid manufacturers
- Product
- 2-Aminobenzothiazole-6-carboxylic acid 93-85-6
- Price
- US $0.00-0.00/KG
- Min. Order
- 1KG
- Purity
- 99.0%
- Supply Ability
- 1000KG
- Release date
- 2024-08-13
- Product
- 2-Aminobenzothiazole-6-carboxylic acid 93-85-6
- Price
- US $36.00-1.50/kg
- Min. Order
- 1kg
- Purity
- 99%
- Supply Ability
- g-kg-tons, free sample is available
- Release date
- 2024-04-09
- Product
- 2-Aminobenzothiazole-6-CarboxylicAcid 93-85-6
- Price
- US $0.00/KG
- Min. Order
- 1KG
- Purity
- 97.5%
- Supply Ability
- 100 tons
- Release date
- 2022-01-14