20061-46-5

Basic information

• Product Name: 5-Benzothiazolecarboxaldehyde,2-methyl-(8CI,9CI)
• Synonyms: 5-Benzothiazolecarboxaldehyde,2-methyl-(8CI,9CI);2-Methyl-benzothiazole-5-carbaldehyde;2-Methyl-1,3-benzothiazole-5-carbaldehyde;2-Methyl-5-benzothiazolecarboxaldehyde
• CAS NO: 20061-46-5
• Molecular Formula: C₉H₇NOS
• Molecular Weight: 177.226
• Product Categories: BENZOTHIAZOLE
• Mol File: 20061-46-5.mol
• Article Data: 8

Chemical Properties

• Melting Point: 100.5 °C(Solv: ligroine (8032-32-4))
• Boiling Point: 316.3±15.0 °C(Predicted)
• Appearance: /
• Density: 1.320±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 0.72±0.10(Predicted)
• CAS DataBase Reference: 5-Benzothiazolecarboxaldehyde,2-methyl-(8CI,9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Benzothiazolecarboxaldehyde,2-methyl-(8CI,9CI)(20061-46-5)
• EPA Substance Registry System: 5-Benzothiazolecarboxaldehyde,2-methyl-(8CI,9CI)(20061-46-5)

Safety Data

• Hazardous Substances Data: 20061-46-5(Hazardous Substances Data)

Usage

General Description

5-Benzothiazolecarboxaldehyde, 2-methyl-(8CI,9CI) is a chemical compound with the molecular formula C9H7NOS. It belongs to the class of organic compounds known as benzothiazoles, which are heterocyclic aromatic compounds containing a benzene and a thiazole ring. This chemical is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It has also been identified as a potential intermediate in the production of dyes, perfumes, and flavoring agents. Additionally, 5-Benzothiazolecarboxaldehyde, 2-methyl-(8CI,9CI) may have potential applications in the development of materials and products for different industrial sectors.

Upstream product

• 24851-69-2 2-methylbenzo[d]thiazole-5-carboxylic acid 
• 35350-37-9 methyl 4-[[4-(methoxycarbonyl)-2-nitrophenyl]disulfanyl]-3-nitrobenzoate 
• 646-06-0 1,3-DIOXOLANE 
• 1006-99-1 2-methyl-5-chloro-benzothiazole 
• 125872-96-0 5-bromomethyl-2-methylbenzothiazole 
• 95-26-1 2,5-dimethylbenzothiazole 
• 74-11-3 para-chlorobenzoic acid 
• 14719-83-6 methyl 3-nitro-4-chlorobenzoate 
• 32770-98-2 2-methyl-5-benzothiazolecarxylic acid methyl ester 
• 96-99-1 4-chloro-3-nitrobenzoate 
• 32770-97-1 (2-methyl-1,3-benzothiazol-5-yl)methanol 

Downstream Products

• 50716-60-4 tetra-N-methyl-4,4'-(2-methyl-benzothiazol-5-ylmethanediyl)-bis-aniline 
• 20077-87-6 1-(2-methylbenzo[d]thiazol-5-yl)ethan-1-ol 
• 50716-64-8 bis-(4-dimethylamino-phenyl)-(2-methyl-benzothiazol-5-yl)-methinium; iodide 
• 20077-88-7 1-(2-methylbenzo[d]thiazol-5-yl)ethan-1-one 
• 924727-12-8 (4S,5R,3'S)-4-methyl-5-phenyl-3-[3'-(2-methylbenzothiazol-5-yl)-3'-hydroxy-2'-oxopropyl]-2-oxazolidinone 
• 16251-45-9 (4S,5R)-4-methyl-5-phenyl-oxazolidin-2-one 

Relevant articles and documents

Mild, Redox-Neutral Formylation of Aryl Chlorides through the Photocatalytic Generation of Chlorine Radicals

We report a redox-neutral formylation of aryl chlorides that proceeds through selective 2-functionalization of 1,3-dioxolane through nickel and photoredox catalysis. This scalable benchtop approach provides a distinct advantage over traditional reductive carbonylation in that no carbon monoxide, pressurized gas, or stoichiometric reductant is employed. The mild conditions give unprecedented scope from abundant and complex aryl chloride starting materials.

GLYCOSIDASE INHIBITORS

Compounds of formula (I) wherein A, R, W, Q, n and m have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.

EPOTHILONE ANALOGUES, THEIR PHARMACEUTICAL COMPOSITIONS, THEIR USE AND THEIR PREPARATIONS

The present invention discloses novel Epothilone analogues, their pharmaceutical compositions, their use and their preparations, especially discloses the compounds of general formula I, their preparations and their use for preparing therapeutical compositions used as cell inhibitors.