O-(Pentachlorophenyl) morpholine-4-carbothioate

Base Information

Chemical Name:O-(Pentachlorophenyl) morpholine-4-carbothioate
CAS No.:100991-59-1
Molecular Formula:C₁₁H₈Cl₅NO₂S
Molecular Weight:395.521
Hs Code.:
DSSTox Substance ID:DTXSID70543616
Wikidata:Q82420549
Mol file:100991-59-1.mol

Synonyms:100991-59-1;O-(Pentachlorophenyl) morpholine-4-carbothioate;DTXSID70543616

Suppliers and Price of O-(Pentachlorophenyl) morpholine-4-carbothioate

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
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Total 0 raw suppliers

Chemical Property of O-(Pentachlorophenyl) morpholine-4-carbothioate

Chemical Property:

XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:394.868888
Heavy Atom Count:20
Complexity:342

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COCCN1C(=S)OC2=C(C(=C(C(=C2Cl)Cl)Cl)Cl)Cl

Technology Process of O-(Pentachlorophenyl) morpholine-4-carbothioate

There total 2 articles about O-(Pentachlorophenyl) morpholine-4-carbothioate 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: 71.0%

: 110-91-8,99108-56-2
morpholine

: 99498-87-0
C₉H₃Cl₇O₂S₂

: 100991-59-1
Morpholine-4-carbothioic acid O-pentachlorophenyl ester

Guidance literature:: In diethyl ether;
DOI:10.1016/S0040-4020(01)87479-2

Reference yield:

: 99498-86-9
C₇Cl₈OS

: 100991-59-1
Morpholine-4-carbothioic acid O-pentachlorophenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / CCl₄ / 50 - 60 °C

2: 71 percent / diethyl ether

In tetrachloromethane; diethyl ether;
DOI:10.1016/S0040-4020(01)87479-2