N,N-Didesmethyl Ulipristal

Base Information

Chemical Name:N,N-Didesmethyl Ulipristal
CAS No.:244206-52-8
Molecular Formula:C₂₆H₃₁NO₃
Molecular Weight:405.537
Hs Code.:
DSSTox Substance ID:DTXSID80579305
Wikidata:Q82469791
Mol file:244206-52-8.mol

Synonyms:N,N-Didesmethyl Ulipristal;244206-52-8;(8S,11R,13S,14S,17R)-17-acetyl-11-(4-aminophenyl)-17-hydroxy-13-methyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one;DTXSID80579305;(11beta)-11-(4-Aminophenyl)-17-hydroxy-19-norpregna-4,9-diene-3,20-dione;J-015512

Suppliers and Price of N,N-Didesmethyl Ulipristal

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
N,N-DidesmethylUlipristal
25mg
$ 10500.00

Biosynth Carbosynth
N,N-Didesmethyl ulipristal
10 mg
$ 6500.00

Biosynth Carbosynth
N,N-Didesmethyl ulipristal
5 mg
$ 3750.00

Biosynth Carbosynth
N,N-Didesmethyl ulipristal
2 mg
$ 1950.00

Biosynth Carbosynth
N,N-Didesmethyl ulipristal
1 mg
$ 1250.00

Total 8 raw suppliers

Chemical Property of N,N-Didesmethyl Ulipristal

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:643.926°C at 760 mmHg
PKA:12.93±0.60(Predicted)
Flash Point:343.234°C
PSA：80.39000
Density:1.25g/cm³
LogP:5.06960
XLogP3:2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:405.23039385
Heavy Atom Count:30
Complexity:833

Purity/Quality:

97% ^*data from raw suppliers

N,N-DidesmethylUlipristal ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1(CCC2C1(CC(C3=C4CCC(=O)C=C4CCC23)C5=CC=C(C=C5)N)C)O
Isomeric SMILES:CC(=O)[C@]1(CC[C@@H]2[C@@]1(C[C@@H](C3=C4CCC(=O)C=C4CC[C@@H]23)C5=CC=C(C=C5)N)C)O

Technology Process of N,N-Didesmethyl Ulipristal

There total 4 articles about N,N-Didesmethyl Ulipristal 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: 1.23%

: 244206-51-7
3,20-bis-ethylenedioxy-5α,17α-dihydroxy-11β-(4-aminophenyl)-19-norpregn-9-ene

: 244206-52-8
11β-(4-aminophenyl)-17α-hydroxy-19-norpregna-4,9-diene-3,20-dione

Guidance literature:: With sulfuric acid; In ethanol; at 95 ℃; for 0.5h;
DOI:10.1016/S0039-128X(98)00086-5

Reference yield:

: 5089-33-8
2-(4-bromophenyl)-1,1,1,3,3,3-hexamethyldisilazane

: 244206-52-8
11β-(4-aminophenyl)-17α-hydroxy-19-norpregna-4,9-diene-3,20-dione

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) Mg, 2.) CuCl, 4.) aq. NH₄Cl

2: 1.23 percent / 8.5 percent aq. H₂SO₄ / ethanol / 0.5 h / 95 °C

With sulfuric acid; ammonium chloride; magnesium; copper(l) chloride; In ethanol;
DOI:10.1016/S0039-128X(98)00086-5

Reference yield:

: 54201-83-1
5α,10α-epoxy-17α-hydroxy-19-norpregn-9(11)-ene-3,20-dione 3,20-bis(ethylene acetal)

: 244206-52-8
11β-(4-aminophenyl)-17α-hydroxy-19-norpregna-4,9-diene-3,20-dione

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) Mg, 2.) CuCl, 4.) aq. NH₄Cl

2: 1.23 percent / 8.5 percent aq. H₂SO₄ / ethanol / 0.5 h / 95 °C

With sulfuric acid; ammonium chloride; magnesium; copper(l) chloride; In ethanol;
DOI:10.1016/S0039-128X(98)00086-5