Dioxopromethazine hydrochloride

Base Information

• Chemical Name: Dioxopromethazine hydrochloride
• CAS No.: 15374-15-9
• Molecular Formula: C₁₇H₂₀N₂O₂S*ClH
• Molecular Weight: 352.885
• UNII: 6XHO7GN8RH
• DSSTox Substance ID: DTXSID40929822
• Wikidata: Q27265673
• Mol file: 15374-15-9.mol

Synonyms:Dioxopromethazine hydrochloride;15374-15-9;6XHO7GN8RH;Dioxopromethazine (hydrochloride);1-(5,5-dioxophenothiazin-10-yl)-N,N-dimethylpropan-2-amine;hydrochloride;Dioxopromethazine hydrochloride [WHO-DD];N-(2-Dimethylaminopropyl)phenothiazine S,S-dioxide hydrochloride;Phenothiazine, 10-(2-(dimethylamino)propyl)-, 5,5-dioxide, monohydrochloride;13754-57-9;Prothanon gel (TN);UNII-6XHO7GN8RH;DTXSID40929822;1ST10324A;AKOS015961656;AC-14455;TS-08866;D07860;J-009047;Q27265673;Promethazine sulfone hydrochloride 100 microg/mL in Acetonitrile;10H-Phenothiazine-10-ethanamine, N,N,alpha-trimethyl-, 5,5-dioxide, hydrochloride (1:1);10H-Phenothiazine-10-ethanamine, N,N,alpha-trimethyl-, 5,5-dioxide, monohydrochloride;10-[2-(Dimethylamino)propyl]-5lambda~6~-phenothiazine-5,5(10H)-dione--hydrogen chloride (1/1);10H-PHENOTHIAZINE-10-ETHANAMINE, N,N,.ALPHA.-TRIMETHYL-, 5,5-DIOXIDE, HYDROCHLORIDE (1:1);10H-PHENOTHIAZINE-10-ETHANAMINE, N,N,.ALPHA.-TRIMETHYL-, 5,5-DIOXIDE, MONOHYDROCHLORIDE;29432-24-4

Chemical Property of Dioxopromethazine hydrochloride

Chemical Property:

• Vapor Pressure: 1.76E-10mmHg at 25°C
• Boiling Point: 502.7oC at 760 mmHg
• Flash Point: 257.8oC
• PSA: 65.92000
• LogP: 4.44790
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 352.1012268
• Heavy Atom Count: 23
• Complexity: 455

Purity/Quality:

98%,99%, ^*data from raw suppliers

DioxopromethazineHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(CN1C2=CC=CC=C2S(=O)(=O)C3=CC=CC=C31)N(C)C.Cl
• Uses: A scheme was developed that allows the detection of dioxopromethazine in a urine sample within 3 min.Dioxopromethazine Hydrochloride is an antihistamine drug.

Technology Process of Dioxopromethazine hydrochloride

There total 2 articles about Dioxopromethazine 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:

Reference yield: 92.3%

9,9-Dioxopromethazin (13582-96-2,13582-97-3,13754-56-8) → dioxopromethazine hydrochloride (13582-95-1,13582-98-4,13754-57-9,15374-15-9,17591-91-2,29432-24-4,13754-56-8)

Guidance literature:

With hydrogenchloride; In acetone; at 20 ℃; for 0.1h; pH=4;

Reference yield:

→ dioxopromethazine hydrochloride (13582-95-1,13582-98-4,13754-57-9,15374-15-9,17591-91-2,29432-24-4,13754-56-8)

Guidance literature:

entspr. Sulfoxid, H2O2;

upstream raw materials:

9,9-Dioxopromethazin

Refernces