- Biomimetic oxidation of some nitrogen-containing compounds by the iodoxybenzene-vanadyl acetylacetonate complexBarret, R.; Pautet, F.; Daudon, M., Pharmazie, 1986, 41(4), 285-6
Cas no 146-21-4 (Promazine Sulfoxide)
Promazine Sulfoxide structure
Product Name:Promazine Sulfoxide
CAS No:146-21-4
MF:C17H20N2OS
MW:300.418502807617
CID:192804
PubChem ID:547559
Update Time:2025-07-29
Promazine Sulfoxide Chemical and Physical Properties
Names and Identifiers
-
- 10H-Phenothiazine-10-propanamine,N,N-dimethyl-, 5-oxide
- 10-[3-(Dimethylamino)propyl]-10H-phenothiazine 5-oxide
- Promazine 5-sulfoxide
- Promazine Sulfoxide
- Phenothiazine, 10-[3-(dimethylamino)propyl]-, 5-oxide
- Promazine, S-oxide
- Propazine sulfoxide
- SKF 5418A
- 10-[3-(dimethylamino)propyl]phenothiazine 5-oxide
- promazine S-oxide
- CHEMBL3544857
- N,N-dimethyl-10H-phenothiazine-10-propanamine 5-oxide
- N,N-dimethyl-3-(5-oxophenothiazin-10-yl)propan-1-amine
- 3-(10H-phenothiazin-10-yl)-N,N-dimethylpropan-1-amine S-oxide
- promazine 5-oxide
- N,N-Dimethyl-3-(5-oxido-10H-phenothiazin-10-yl)-1-propanamine #
- 10-[3-(dimethylamino)propyl]-5lambda(4)-phenothiazin-5(10H)-one
- N,N-dimethyl-3-(5-oxido-10H-phenothiazin-10-yl)propan-1-amine
- KSHDHDWHIWBNHA-UHFFFAOYSA-N
- Promazine Sulphoxide 1.0 mg/ml in Methanol
- propazin sulfoxide
- CHEBI:145225
- Promazine Hydrochloride Imp. A (EP); Promazine Imp. A (EP); 3-(10H-Phenothiazin-10-yl)-N,N-dimethylpropan-1-amine S-Oxide; Promazine Sulphoxide; Promazine Hydrochloride Impurity A; Promazine Impurity A
- NS00113795
- 10H-Phenothiazine-10-propanamine, N,N-dimethyl-, 5-oxide
- DTXSID301021656
- 10-[3-(dimethylamino)propyl]-10H-5$l^{4},10-phenothiazin-5-one
- Promazine Sulphoxide
- 146-21-4
- 3-(10H-Phenothiazin-10-yl)-N,N-dimethylpropan-1-amine S-Oxide (Promazine Sulphoxide)
-
- Inchi： 1S/C17H20N2OS/c1-18(2)12-7-13-19-14-8-3-5-10-16(14)21(20)17-11-6-4-9-15(17)19/h3-6,8-11H,7,12-13H2,1-2H3
- InChI Key： KSHDHDWHIWBNHA-UHFFFAOYSA-N
- SMILES： S1(C2C=CC=CC=2N(C2C=CC=CC1=2)CCCN(C)C)=O
Computed Properties
- Exact Mass: 300.1298
- Monoisotopic Mass: 300.13
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 21
- Rotatable Bond Count: 4
- Complexity: 348
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 3.3
- Topological Polar Surface Area: 53.5A^2
Experimental Properties
- PSA: 23.55
Promazine Sulfoxide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | P756310-5mg |
Promazine Sulfoxide |
146-21-4 | 5mg |
$ 94.00 | 2023-09-06 | ||
| TRC | P756310-10mg |
Promazine Sulfoxide |
146-21-4 | 10mg |
$ 167.00 | 2023-04-15 | ||
| TRC | P756310-25mg |
Promazine Sulfoxide |
146-21-4 | 25mg |
$ 374.00 | 2023-04-15 | ||
| TRC | P756310-50mg |
Promazine Sulfoxide |
146-21-4 | 50mg |
$ 666.00 | 2023-04-15 | ||
| TRC | P756310-100mg |
Promazine Sulfoxide |
146-21-4 | 100mg |
$ 1183.00 | 2023-04-15 | ||
| A2B Chem LLC | AF12922-5mg |
10-[3-(Dimethylamino)propyl]-10H-phenothiazine 5-oxide |
146-21-4 | 5mg |
$212.00 | 2024-04-20 |
Promazine Sulfoxide Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Iodylbenzene , Vanadyl acetylacetonate Solvents: Benzene
Reference
Promazine Sulfoxide Raw materials
Promazine Sulfoxide Preparation Products
Promazine Sulfoxide Related Literature
-
M. Hor?ic,J. Svoboda,V. Novotná,D. Pociecha,E. Gorecka Chem. Commun. 2017 53 2721
-
2. Olefin synthesis by two-fold extrusion processes. Part II. Synthesis of some very hindered olefinsDerek H. R. Barton,Frank S. Guziec,Israel Shahak J. Chem. Soc. Perkin Trans. 1 1974 1794
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