16,16-Dimethylprostaglandin A1

Base Information

Chemical Name:16,16-Dimethylprostaglandin A1
CAS No.:41692-24-4
Molecular Formula:C₂₂H₃₆O₄
Molecular Weight:364.525
Hs Code.:
UNII:5668IJK40E
DSSTox Substance ID:DTXSID401347768
Metabolomics Workbench ID:2444
Wikidata:Q27261379
Mol file:41692-24-4.mol

Synonyms:16,16-diMe-PGA1;16,16-dimethylprostaglandin A1;dmPGA1

Suppliers and Price of 16,16-Dimethylprostaglandin A1

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
16,16-DimethylProstaglandinA1
2.5mg
$ 130.00

Cayman Chemical
16,16-dimethyl Prostaglandin A1 ≥98%
10mg
$ 560.00

Cayman Chemical
16,16-dimethyl Prostaglandin A1 ≥98%
1mg
$ 70.00

Cayman Chemical
16,16-dimethyl Prostaglandin A1 ≥98%
5mg
$ 315.00

AK Scientific
16,16-DimethylprostaglandinA1
1mg
$ 194.00

AK Scientific
16,16-DimethylprostaglandinA1
5mg
$ 525.00

AHH
16,16-DimethylprostaglandinA1 98%
0.01g
$ 388.00

Total 2 raw suppliers

Chemical Property of 16,16-Dimethylprostaglandin A1

Chemical Property:

Vapor Pressure:4.01E-13mmHg at 25°C
Boiling Point:523°Cat760mmHg
Flash Point:284.2°C
PSA：74.60000
Density:1.063g/cm³
LogP:4.91640
XLogP3:5.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:13
Exact Mass:364.26135963
Heavy Atom Count:26
Complexity:504

Purity/Quality:

≥98% ^*data from raw suppliers

16,16-DimethylProstaglandinA1 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCC(C)(C)C(C=CC1C=CC(=O)C1CCCCCCC(=O)O)O
Isomeric SMILES:CCCCC(C)(C)[C@@H](/C=C/[C@H]1C=CC(=O)[C@@H]1CCCCCCC(=O)O)O
Uses 16,16-dimethyl Prostaglandin A1 is a metabolism resistant analog of PGA1.

Technology Process of 16,16-Dimethylprostaglandin A1

There total 2 articles about 16,16-Dimethylprostaglandin A1 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:

: 41692-15-3
16,16-Dimethylprostaglandin E1

: 41692-24-4
16.16-Dimethyl-PGA1

Guidance literature:: With acetic acid;

Reference yield:

: 7-[(1R,2R,3R,5S)-2-[(E)-(R)-4,4-Dimethyl-3-(tetrahydro-pyran-2-yloxy)-oct-1-enyl]-5-hydroxy-3-(tetrahydro-pyran-2-yloxy)-cyclopentyl]-heptanoic acid

: 41692-24-4
16.16-Dimethyl-PGA1

Guidance literature:: Multi-step reaction with 2 steps

1: (i) CrO₃, aq. MnSO₄, H₂SO₄, (ii) AcOH, THF

2: acetic acid

With acetic acid;