70590-48-6

Basic information

• Product Name: 4(5H)-Benzothiazolone, 6,7-dihydro-
• Synonyms: 4(5H)-Benzothiazolone, 6,7-dihydro-
• CAS NO: 70590-48-6
• Molecular Formula: C7H7NOS
• Molecular Weight: 153.2
• Mol File: 70590-48-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 298.3±9.0 °C(Predicted)
• Appearance: /
• Density: 1.326±0.06 g/cm3(Predicted)
• PKA: 0.48±0.20(Predicted)
• CAS DataBase Reference: 4(5H)-Benzothiazolone, 6,7-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 4(5H)-Benzothiazolone, 6,7-dihydro-(70590-48-6)
• EPA Substance Registry System: 4(5H)-Benzothiazolone, 6,7-dihydro-(70590-48-6)

Safety Data

• Hazardous Substances Data: 70590-48-6(Hazardous Substances Data)

Upstream product

• 95203-30-8 ethyl 4,5,6,7-tetrahydrobenzothiazole-5-carboxylate 
• 70590-45-3 5-(3-ethoxycarbonyl-propyl)-thiazole-4-carboxylic acid ethyl ester 
• 42212-75-9 diethyl 2-oxopimelate 
• 70590-46-4 bromo-3 oxo-2 pimelate d'ethyle 
• 765-87-7 cyclohexane-1,2-dione 
• 24829-91-2 3-bromocyclohexane-1,2-dione 
• 36234-66-9 2-amino-6,7-dihydrobenzo[d]thiazol-4(5H)-one 

Relevant articles and documents

COMPOUNDS AND METHODS FOR TREATING CANCER

Substituted hydrazone compounds, methods of making such compounds and metal complexes thereof, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds and metal complexes to treat, prevent or ameliorate cancer are provided.

New benzo [d] thiazole derivatives, process for their preparation and their therapeutic applications

This invention relates to compounds having the general formula: STR1 and their pharmaceutically acceptable acid addition salts having the formula: STR2 in which: R represents hydrogen or a C1-4 alkyl radical, R' represents hydrogen or a C1-4 alkyl radical, m is 0, 1, 2 or 3, n is 3, 2, 1 or 0, the sum m+n being always equal to 3, and X- represents an anion formed by a pharmaceutically acceptable acid. Said compounds are typically useful as analgesic agents and as stimulants of the sympathetic nervous system, and also as central and peripheral vasoregulator agents.