10H-Pyrido(3,2-b)(1,4)benzothiazine-10-carbothioic acid, S-(3-diisopropylaminopropyl) ester

Base Information

Chemical Name:10H-Pyrido(3,2-b)(1,4)benzothiazine-10-carbothioic acid, S-(3-diisopropylaminopropyl) ester
CAS No.:63906-32-1
Molecular Formula:C₂₁H₂₇N₃OS₂
Molecular Weight:401.597
Hs Code.:
DSSTox Substance ID:DTXSID90213566
Nikkaji Number:J85.750E
Wikidata:Q83089023

Synonyms:D 265;63906-32-1;BRN 1034543;10H-Pyrido(3,2-b)(1,4)benzothiazine-10-carbothioic acid, S-(3-diisopropylaminopropyl) ester;C21H27N3OS2;DTXSID90213566;LS-133158;10H-Pyrido[3,2-b][1,4]benzothiazine-10-carbothioic acid, S-[3-[bis(1-methylethyl)amino]propyl] ester

Suppliers and Price of 10H-Pyrido(3,2-b)(1,4)benzothiazine-10-carbothioic acid, S-(3-diisopropylaminopropyl) ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
S-[3-(DIISOPROPYLAMINO)PROPYL]-10H-PYRIDO-[3,2-B]-[1,4]BENZOTHIAZINE-10-CARBOTHIOIC ACID ESTER 95.00%
5MG
$ 501.13

Total 0 raw suppliers

Chemical Property of 10H-Pyrido(3,2-b)(1,4)benzothiazine-10-carbothioic acid, S-(3-diisopropylaminopropyl) ester

Chemical Property:

Vapor Pressure:4.22E-11mmHg at 25°C
Boiling Point:524.7°C at 760 mmHg
Flash Point:271.1°C
PSA：87.04000
Density:1.198g/cm³
LogP:6.11140
XLogP3:5.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:7
Exact Mass:401.15955484
Heavy Atom Count:27
Complexity:480

Purity/Quality:: S-[3-(DIISOPROPYLAMINO)PROPYL]-10H-PYRIDO-[3,2-B]-[1,4]BENZOTHIAZINE-10-CARBOTHIOIC ACID ESTER 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)N(CCCSC(=O)N1C2=CC=CC=C2SC3=C1N=CC=C3)C(C)C

Technology Process of 10H-Pyrido(3,2-b)(1,4)benzothiazine-10-carbothioic acid, S-(3-diisopropylaminopropyl) ester

There total 2 articles about 10H-Pyrido(3,2-b)(1,4)benzothiazine-10-carbothioic acid, S-(3-diisopropylaminopropyl) ester 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:

: 261-96-1
1-azaphenothiazine

: 63906-32-1
4-Aza-phenothiazin-10-carbonsaeure-3-<1-diisopropylamino-propylthioester>

Guidance literature:: Multi-step reaction with 2 steps

1: HCl / chlorobenzene / 170 °C

2: chlorobenzene / Heating

With hydrogenchloride; In chlorobenzene;