6-Acetylthiomorphine

Base Information

Chemical Name:6-Acetylthiomorphine
CAS No.:117152-64-4
Molecular Formula:C₁₉H₂₁NO₃S
Molecular Weight:343.447
Hs Code.:
DSSTox Substance ID:DTXSID30151711
Nikkaji Number:J227.496E
Wikidata:Q83018247
Mol file:117152-64-4.mol

Synonyms:(-)-6beta-acetylthionormorphine;6-acetylthiomorphine;KT 88;KT-88

Suppliers and Price of 6-Acetylthiomorphine

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

Total 0 raw suppliers

Chemical Property of 6-Acetylthiomorphine

Chemical Property:

Vapor Pressure:6.77E-11mmHg at 25°C
Boiling Point:506.9°Cat760mmHg
Flash Point:260.3°C
PSA：75.07000
Density:1.41g/cm³
LogP:2.42340
XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:343.12421471
Heavy Atom Count:24
Complexity:595

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)SC1C=CC2C3CC4=C5C2(C1OC5=C(C=C4)O)CCN3C
Isomeric SMILES:CC(=O)S[C@@H]1C=C[C@H]2[C@H]3CC4=C5[C@]2([C@H]1OC5=C(C=C4)O)CCN3C

Technology Process of 6-Acetylthiomorphine

There total 1 articles about 6-Acetylthiomorphine 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: 30.0%

: 507-09-5
tiolacetic acid

: 57-27-2
MORPHIN

: 22222-94-2
3-acetoxy-6β-acetylsulfanyl-4,5α-epoxy-17-methyl-morphin-7-ene

: 117152-64-4
C₁₉H₂₁NO₃S

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 ℃;
DOI:10.1248/cpb.36.2282

Reference yield:

: 117152-64-4
C₁₉H₂₁NO₃S

: 119931-37-2
C₂₃H₂₂N₂O₄S₂

Guidance literature:: Multi-step reaction with 2 steps

1: 66 percent / potassium hydroxide / ethanol

2: 79 percent / acetonitrile / 0 °C

With potassium hydroxide; In ethanol; acetonitrile;
DOI:10.1248/cpb.36.2282