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Gaboxadol hydrochloride

Base Information Edit
  • Chemical Name:Gaboxadol hydrochloride
  • CAS No.:64603-91-4
  • Molecular Formula:C6H8 N2 O2
  • Molecular Weight:140.142
  • Hs Code.:
  • European Community (EC) Number:285-687-7
  • NSC Number:759585
  • UNII:478RVH3TVD
  • DSSTox Substance ID:DTXSID90234251
  • Wikidata:Q27259031
  • ChEMBL ID:CHEMBL1255746
  • Mol file:64603-91-4.mol
Gaboxadol hydrochloride

Synonyms:GABOXADOL HYDROCHLORIDE;THIP hydrochloride;85118-33-8;Gaboxadol (hydrochloride);Gaboxadol HCl;UNII-478RVH3TVD;478RVH3TVD;85118-33-8 (HCl);4,5,6,7-Tetrahydroisoxazolo[5,4-c]pyridin-3-ol hydrochloride;4,5,6,7-Tetrahydroisoxazolo(5,4-c)pyridin-3(2H)-one monohydrochloride;EINECS 285-687-7;4,5,6,7-Tetrahydroisoxazolo[5,4-c]pyridin-3(2H)-one hydrochloride;4,5,6,7-TETRAHYDROISOXAZOLO[5,4-C]PYRIDIN-3-OL HCL, GABOXADOL-HCL;Lu 02-030 (hydrochloride);THIP (hydrochloride);4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridin-3(2H)-one monohydrochloride;SR-01000075651;4,5,6,7-Tetrahydro-isoxazolo[5,4-c]pyridin-3(2H)-one;4,5,6,7-Tetrahydroisoxazolo(5,4-c)pyridin-3(2H)-one hydrate;THIP HCl;(THIP);D00XNY;MLS002154080;SPECTRUM1503648;CHEMBL1255746;DTXSID90234251;HMS1571C05;Pharmakon1600-01503648;BCP16610;GABOXADOL HYDROCHLORIDE [MI];Tox21_501233;CCG-39368;MFCD00055180;NSC759585;AKOS024015212;LP01233;NCGC00094475-01;NCGC00094475-02;NCGC00094475-03;NCGC00094475-04;NCGC00261918-01;AS-53745;BP-12453;HY-10233;SMR000875361;J Med Chem 26: 895 (1983);CS-0002508;EU-0101233;G0405;T-101;EN300-152453;P17040;Gaboxadol hydrochloride, solid, >=98% (HPLC);SR-01000075651-1;SR-01000075651-3;SR-01000075651-6;SR-01000075651-7;4,5,6,7-tetrahydroisoxazolo-[5,4-c]-pyridin-3-ol;Q27259031;9-Oxa-3,8-Diazabicyclo[4.3.0]Non-10-En-7-one HCl;Z2688689710;4H,5H,6H,7H-[1,2]oxazolo[5,4-c]pyridin-3-ol hydrochloride;4,5,6,7-Tetrahydroisoxazolo[5,4-c]pyridin-3(2H)-onehydrochloride;4,5,6,7-tetrahydro-[1,2]oxazolo[5,4-c]pyridin-3-one;hydrochloride;ISOXAZOLO(5,4-C)PYRIDIN-3(2H)-ONE, 4,5,6,7-TETRAHYDRO-, HYDROCHLORIDE (1:1);ISOXAZOLO(5,4-C)PYRIDIN-3(2H)-ONE, 4,5,6,7-TETRAHYDRO-, MONOHYDROCHLORIDE

Suppliers and Price of Gaboxadol hydrochloride
Supply Marketing:Edit
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
  • Usbiological
  • THIP hydrochloride
  • 50mg
  • $ 403.00
  • Tocris
  • THIPhydrochloride ≥98%(HPLC)
  • 50
  • $ 162.00
  • ChemScene
  • THIP 99.36%
  • 25mg
  • $ 90.00
  • Biorbyt Ltd
  • THPO
  • 10 μg
  • $ 290.70
  • American Custom Chemicals Corporation
  • GABOXADOL 95.00%
  • 50MG
  • $ 685.21
Total 79 raw suppliers
Chemical Property of Gaboxadol hydrochloride Edit
Chemical Property:
  • Appearance/Colour:white solid 
  • Vapor Pressure:0.00113mmHg at 25°C 
  • Melting Point:242-244° (dec) 
  • Boiling Point:340.5 °C at 760 mmHg 
  • PKA:pKa (water, 25°): 4.44 ±0.03; 8.48 ±0.04 
  • Flash Point:159.7 °C 
  • PSA:58.29000 
  • Density:1.36 g/cm3 
  • LogP:1.15670 
  • Storage Temp.:Store at RT 
  • Solubility.:ethanol: 0.91 mg/mL 
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:176.0352552
  • Heavy Atom Count:11
  • Complexity:210
Purity/Quality:

98%,99%, *data from raw suppliers

THIP hydrochloride *data from reagent suppliers

Safty Information:
  • Pictogram(s): A poison. 
  • Hazard Codes:A poison. 
  • Safety Statements: 22-24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CNCC2=C1C(=O)NO2.Cl
  • Description Gaboxadol HCl (64603-91-4) is a GABA-A receptor agonist. Hypnotic agent.
  • Uses GABAa agonist, GABAc antagonist
Technology Process of Gaboxadol hydrochloride

There total 4 articles about Gaboxadol hydrochloride 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:
Guidance literature:
With triethylamine; In ethanol; water; at 5 ℃; for 2h;
Guidance literature:
With triethylamine; In ethanol; water; hydrogen bromide; acetic acid;
Refernces Edit
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