17229-76-4

Basic information

• Product Name: Benzothiazole, 2-propyl- (6CI,7CI,8CI,9CI)
• Synonyms: Benzothiazole, 2-propyl- (6CI,7CI,8CI,9CI);Benzothiazole, 2-propyl-;2-Propylbenzthiazole;2-Propyl-1,3-benzothiazole;2-Propylbenzo[d]thiazole
• CAS NO: 17229-76-4
• Molecular Formula: C₁₀H₁₁NS
• Molecular Weight: 177.26604
• Product Categories: BENZOTHIAZOLE
• Mol File: 17229-76-4.mol
• Article Data: 54

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Benzothiazole, 2-propyl- (6CI,7CI,8CI,9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzothiazole, 2-propyl- (6CI,7CI,8CI,9CI)(17229-76-4)
• EPA Substance Registry System: Benzothiazole, 2-propyl- (6CI,7CI,8CI,9CI)(17229-76-4)

Safety Data

• Hazardous Substances Data: 17229-76-4(Hazardous Substances Data)

Usage

General Description

Benzothiazole, 2-propyl- is a chemical compound with the molecular formula C11H13NS. It is a organic compound with a benzene ring fused to a thiazole ring, and a propyl substituent attached to the nitrogen atom. This chemical is used primarily as a synthetic intermediate in the production of various pharmaceuticals, pesticides, and other organic compounds. It is also known for its use as a rubber accelerator, corrosion inhibitor, and fragrance ingredient. Benzothiazole, 2-propyl- is considered to be a potential environmental contaminant and is regulated for its impact on human health and the environment.

Upstream product

• 18051-60-0 N-phenylthiobutyramide 
• 98370-54-8 zinc 2-aminobenzenethiolate 
• 141-75-3 butyryl chloride 
• 107-92-6 butyric acid 
• 137-07-5 2-amino-benzenethiol 
• 5796-97-4 bis(triethylsilyl) peroxide 
• 125414-91-7 (2-Benzothiazolyl)methyllithium 
• 905-97-5 N,N'-diethylthiacarbocyanine iodide 
• 909-63-7 3,3',9-triethylthiacarbocyanine iodide 
• 61878-83-9 3,3'-diethyl-9-methoxythiacarbocyanine iodide 
• 3065-79-0 3-ethyl-2-[3-(3-ethyl-3H-2-benzothiazolylidene)-2-methyl-1-propenyl] benzothiazolium iodide 
• 61878-84-0 3,3'-diethyl-9-aminothiacarbocyanine iodide 
• 905-97-5 3,3'-diethylthiacarbocyanine iodide 
• 62630-96-0 2-{(Z)-2-Ethoxy-3-[3-ethyl-3H-benzothiazol-(2Z)-ylidene]-propenyl}-3-ethyl-benzothiazol-3-ium; iodide 

Downstream Products

• 17626-87-8 2-(sec-butyl)benzo[d]thiazole 
• 125414-98-4 2-(1-Trimethylsilanyloxy-propyl)-benzothiazole 
• 91258-42-3 C₃₆H₅₂N₂S₂ 
• 111982-01-5 1-phenyl-2-(2-benzothiazolyl)butan-1-ol 
• 111982-01-5 1-phenyl-2-(2-benzothiazolyl)butan-1-ol 
• 101345-85-1 C₃₆H₅₂N₂S₂ 
• 95-16-9 1,3-Benzothiazole 
• 1629-78-3 2-acetylbenzothiazole 

Relevant articles and documents

A biomass-derived N-doped porous carbon catalyst for the aerobic dehydrogenation of nitrogen heterocycles

N-doped porous carbon (NC) was synthesized from sugar cane bagasse, which is a sustainable and widely available biomass waste. The preferred NC sample had a well-developed porous structure, a graphene-like surface morphology and different N species. More

Method for preparing N - heterocyclic ring through visible light mediated dehydrogenation

The invention discloses a method for preparing N - heterocyclic rings through visible light mediated dehydrogenation, and the reaction can be carried out under the conditions of room temperature and visible light without heating. The novel tetra-coordination N-N - diaryl chelating borate compound serves as a photocatalyst, so that the use of a noble metal photocatalyst is avoided, precious metal residue in the reaction product can be reduced as much as possible, and the method is more suitable for synthesizing bioactive molecules.

Method for preparing alkyl benzothiazole derivative under visible light

The invention discloses a method for preparing an alkyl benzothiazole derivative under visible light, which specifically comprises the following steps: under the protection of inert gas, adding N-(2-bromophenyl) alkyl thioamide and inorganic base into a reaction container provided with a stirring device, then adding dimethyl sulfoxide, stirring and reacting for 24 hours at room temperature under the irradiation of visible light, and obtaining the alkyl benzothiazole derivative. Under the condition of not adding any photosensitizer or transition metal catalyst, sodium phosphate is used as alkali, and under the irradiation of a 45W household compact fluorescent lamp, a series of intramolecular cross-coupling reactions of N-(2-bromophenyl) alkyl thioamide are realized. In addition, the alkylbenzothiazole derivative can be obtained with high yield. The whole process is green, efficient and easy to operate, and the method is a good method for synthesizing the alkylbenzothiazole derivative.