2,3-Dinor-6-oxoprostaglandin F1alpha

Base Information

Chemical Name:2,3-Dinor-6-oxoprostaglandin F1alpha
CAS No.:64700-71-6
Molecular Formula:C₁₈H₃₀O₆
Molecular Weight:342.433
Hs Code.:
DSSTox Substance ID:DTXSID301314213
Nikkaji Number:J246.646E
Wikidata:Q27144266
NCI Thesaurus Code:C126898
Metabolomics Workbench ID:2447
Mol file:64700-71-6.mol

Synonyms:2,3-dinor-6-keto-PGF1alpha;2,3-dinor-6-ketoprostaglandin F1alpha;2,3-dinor-6-oxo-PGF1alpha;2,3-dinor-6-oxoprostaglandin F1alpha;2,3-DKPGF1alpha;PGI2-M

Suppliers and Price of 2,3-Dinor-6-oxoprostaglandin F1alpha

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

TRC
2,3-Dinor-6-ketoProstaglandinF1α
10mg
$ 3300.00

TRC
2,3-Dinor-6-ketoProstaglandinF1α
5mg
$ 2200.00

American Custom Chemicals Corporation
2,3-DINOR-6-KETO PROSTAGLANDIN F1ALPHA 95.00%
5MG
$ 504.65

Total 7 raw suppliers

Chemical Property of 2,3-Dinor-6-oxoprostaglandin F1alpha

Chemical Property:

Vapor Pressure:7.5E-14mmHg at 25°C
Boiling Point:538.7 °C at 760 mmHg
Flash Point:293.7 °C
PSA：115.06000
Density:1.232 g/cm³
LogP:1.66570
XLogP3:0.7
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:11
Exact Mass:342.20423867
Heavy Atom Count:24
Complexity:433

Purity/Quality:

99% ^*data from raw suppliers

2,3-Dinor-6-ketoProstaglandinF1α ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCC(C=CC1C(CC(C1CC(=O)CCC(=O)O)O)O)O
Isomeric SMILES:CCCCC[C@@H](/C=C/[C@H]1[C@@H](C[C@@H]([C@@H]1CC(=O)CCC(=O)O)O)O)O
Uses A metabolite of Prostaglandin A metabolite of Prostaglandin (P838600).

Technology Process of 2,3-Dinor-6-oxoprostaglandin F1alpha

There total 13 articles about 2,3-Dinor-6-oxoprostaglandin F1alpha 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:

: 2,3-dinor-6-oxo-PGF(1α), 6.9-hemiacetal, 1,6-lactone

: 64700-71-6
2,3-dinor-6-keto-prostaglandin F_1a

Guidance literature:: Multi-step reaction with 2 steps

1: water; acetic acid / tetrahydrofuran / 60 h / 45 °C

2: acetic acid / water

With water; acetic acid; In tetrahydrofuran; water;

Reference yield:

: 82290-18-4
(1S,2R,3R,4R)-2-((Z)-5-Hydroxy-pent-2-enyl)-4-(tetrahydro-pyran-2-yloxy)-3-[(E)-(S)-3-(tetrahydro-pyran-2-yloxy)-oct-1-enyl]-cyclopentanol

: 64700-71-6
2,3-dinor-6-keto-prostaglandin F_1a

Guidance literature:: Multi-step reaction with 9 steps

1.1: 1H-imidazole / N,N-dimethyl-formamide / 3 h / -78 - -15 °C

2.1: sodium hydrogencarbonate; iodine / dichloromethane / 0.95 h / 5 - 10 °C

3.1: DBN / benzene / 20 h / 45 °C / Inert atmosphere

4.1: potassium hydrogensulfate / diethyl ether / 4.5 h / 20 °C

5.1: dmap; pyridine / 1.5 h / 20 °C

6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 5.5 h / 20 °C / Inert atmosphere

7.1: Jones reagent / acetone / 1 h / -30 - -16 °C

7.2: 0.05 h / 20 °C

7.3: 3.5 h / 45 °C

8.1: sodium hydroxide / water; tert-butyl alcohol / 1.5 h / 20 °C

9.1: acetic acid / water

With pyridine; 1H-imidazole; dmap; potassium hydrogensulfate; Jones reagent; DBN; tetrabutyl ammonium fluoride; iodine; sodium hydrogencarbonate; acetic acid; sodium hydroxide; In tetrahydrofuran; diethyl ether; dichloromethane; water; N,N-dimethyl-formamide; acetone; tert-butyl alcohol; benzene;

Reference yield:

: C₃₄H₆₁IO₆Si

: 64700-71-6
2,3-dinor-6-keto-prostaglandin F_1a

Guidance literature:: Multi-step reaction with 7 steps

1.1: DBN / benzene / 20 h / 45 °C / Inert atmosphere

2.1: potassium hydrogensulfate / diethyl ether / 4.5 h / 20 °C

3.1: dmap; pyridine / 1.5 h / 20 °C

4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 5.5 h / 20 °C / Inert atmosphere

5.1: Jones reagent / acetone / 1 h / -30 - -16 °C

5.2: 0.05 h / 20 °C

5.3: 3.5 h / 45 °C

6.1: sodium hydroxide / water; tert-butyl alcohol / 1.5 h / 20 °C

7.1: acetic acid / water

With pyridine; dmap; potassium hydrogensulfate; Jones reagent; DBN; tetrabutyl ammonium fluoride; acetic acid; sodium hydroxide; In tetrahydrofuran; diethyl ether; water; acetone; tert-butyl alcohol; benzene;