10H-Pyrido(3,2-b)(1,4)benzothiazine, 10-(2-(dibutylamino)ethyl)-

Base Information

• Chemical Name: 10H-Pyrido(3,2-b)(1,4)benzothiazine, 10-(2-(dibutylamino)ethyl)-
• CAS No.: 67465-65-0
• Molecular Formula: C21H29N3S
• Molecular Weight: 355.54
• DSSTox Substance ID: DTXSID90217807
• Nikkaji Number: J85.756D
• Wikidata: Q83094469

Synonyms:10H-Pyrido(3,2-b)(1,4)benzothiazine, 10-(2-(dibutylamino)ethyl)-;67465-65-0;D 216;BRN 1086620;N-butyl-N-(2-pyrido[3,2-b][1,4]benzothiazin-10-ylethyl)butan-1-amine;DTXSID90217807;LS-133215;10-(2-Dibutylaminoethyl)-10H-pyrido[3,2-b][1,4]benzothiazine;10H-Pyrido[3,2-b][1,4]benzothiazine-10-ethanamine, N,N-dibutyl-

Chemical Property of 10H-Pyrido(3,2-b)(1,4)benzothiazine, 10-(2-(dibutylamino)ethyl)-

Chemical Property:

• Vapor Pressure: 1.23E-09mmHg at 25°C
• Boiling Point: 487°C at 760 mmHg
• Flash Point: 248.4°C
• PSA: 44.67000
• Density: 1.088g/cm³
• LogP: 5.65150
• XLogP3: 5.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 9
• Exact Mass: 355.20821911
• Heavy Atom Count: 25
• Complexity: 370

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCN(CCCC)CCN1C2=CC=CC=C2SC3=C1N=CC=C3

Technology Process of 10H-Pyrido(3,2-b)(1,4)benzothiazine, 10-(2-(dibutylamino)ethyl)-

There total 2 articles about 10H-Pyrido(3,2-b)(1,4)benzothiazine, 10-(2-(dibutylamino)ethyl)- 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:

2-(phenylamino)pyridine (6631-37-4) → 10-<2-Dibutylamino-aethyl>-4-aza-phenothiazin (67465-65-0)

Guidance literature:

Multi-step reaction with 2 steps

1: sulfur, I₂ / 250 - 335 °C

2: NaNH₂

With iodine; sulfur; sodium amide;

Reference yield:

1-azaphenothiazine (261-96-1) + N-(2-dibutylamino)ethyl chloride (13422-90-7) → 10-<2-Dibutylamino-aethyl>-4-aza-phenothiazin (67465-65-0)

Guidance literature:

With sodium amide;

upstream raw materials:

1-azaphenothiazine

N-(2-dibutylamino)ethyl chloride

2-(phenylamino)pyridine

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