3-(Methylamino)-2,1-benzisothiazole

Base Information

• Chemical Name: 3-(Methylamino)-2,1-benzisothiazole
• CAS No.: 700-07-2
• Molecular Formula: C₈H₈N₂S
• Molecular Weight: 164.231
• UNII: DVJ526480G
• DSSTox Substance ID: DTXSID301343620
• Nikkaji Number: J629.900H
• Wikidata: Q82924566
• Mol file: 700-07-2.mol

Synonyms:3-(Methylamino)-2,1-benzisothiazole;CI 624;N-Methyl-2,1-benzisothiazol-3-amine;BRN 1072758;2,1-Benzisothiazole, 3-(methylamino)-;DVJ526480G;CI-624;700-07-2;CCRIS 8333;3-(Methylamino)-2,1-benisothiazole;2,1-Benzisothiazol-3-amine, N-methyl-, monohydrochloride;UNII-DVJ526480G;SCHEMBL18879073;CI624;DTXSID301343620;AKOS014777053;2,1-Benzisothiazol-3-amine, N-methyl-;LS-33571;LS-190732

Chemical Property of 3-(Methylamino)-2,1-benzisothiazole

Chemical Property:

• Vapor Pressure: 0.000667mmHg at 25°C
• Refractive Index: 1.73
• Boiling Point: 308.8 °C at 760 mmHg
• Flash Point: 140.5 °C
• Density: 1.306 g/cm³
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 164.04081944
• Heavy Atom Count: 11
• Complexity: 140

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CNC1=C2C=CC=CC2=NS1

Technology Process of 3-(Methylamino)-2,1-benzisothiazole

There total 1 articles about 3-(Methylamino)-2,1-benzisothiazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ 3-Methylamino-<2,1>benzisothiazol (700-07-2)

Guidance literature:

2-Amino-thiobenzoesaeure-methylamid/Pyridin,30percentig.H2O2;35gradC;

DOI:10.1021/jm00328a024