O-(4-formylphenyl) N,N-dimethylcarbamothioate

Base Information

Chemical Name:O-(4-formylphenyl) N,N-dimethylcarbamothioate
CAS No.:84265-06-5
Molecular Formula:C₁₀H₁₁NO₂S
Molecular Weight:209.269
Hs Code.:
DSSTox Substance ID:DTXSID501254619
Mol file:84265-06-5.mol

Synonyms:84265-06-5;1-(4-Formylphenoxy)-N,N-dimethylmethanethioamide;O-(4-formylphenyl) N,N-dimethylcarbamothioate;1-4-formylphenoxy-N,N-dimethylmethanethioamide;O-(4-Formylphenyl)carbamothioicaciddimethylester;O-(4-formylphenyl) dimethylcarbamothioate;SCHEMBL9320116;DTXSID501254619;O-(4-formylphenyl) dimethylthiocarbamate;CS-0233804;EN300-136236;AA-516/31407030;Z1269234310;O-(4-FORMYLPHENYL)CARBAMOTHIOIC ACID DIMETHYL ESTER

Suppliers and Price of O-(4-formylphenyl) N,N-dimethylcarbamothioate

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
1-(4-formylphenoxy)-N,N-dimethylmethanethioamide
250mg
$ 350.00

American Custom Chemicals Corporation
O-(4-FORMYLPHENYL) DIMETHYLTHIOCARBAMATE 95.00%
5MG
$ 498.62

Total 5 raw suppliers

Chemical Property of O-(4-formylphenyl) N,N-dimethylcarbamothioate

Chemical Property:

PSA：61.63000
LogP:1.72440
XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:209.05104977
Heavy Atom Count:14
Complexity:210

Purity/Quality:

99% ^*data from raw suppliers

1-(4-formylphenoxy)-N,N-dimethylmethanethioamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)C(=S)OC1=CC=C(C=C1)C=O

Technology Process of O-(4-formylphenyl) N,N-dimethylcarbamothioate

There total 2 articles about O-(4-formylphenyl) N,N-dimethylcarbamothioate 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: 92.0%

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 16420-13-6
N,N-Dimethylthiocarbamoyl chloride

: 84265-06-5
O-(4-formylphenyl) dimethylcarbamothioate

Guidance literature:: In dichloromethane;
DOI:10.1039/d1tb01721g

Reference yield:

: 19654-38-7
N,N-dimethyl[(4-formylphenyl)thio]formamide

: 69251-24-7
[1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-ethyl]-triphenylphosphonium bromide

: 84265-05-4
S-[p-[2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)propenyl]phenyl]dimethylthiocarbamate

: 84265-06-5
O-(4-formylphenyl) dimethylcarbamothioate

Guidance literature:: In tetrahydrofuran; methanol; hexane; water; ethyl acetate;

Reference yield:

: 84265-06-5
O-(4-formylphenyl) dimethylcarbamothioate

: S-(4-formylphenyl)methanesulfonothioate

Guidance literature:: Multi-step reaction with 3 steps

1: 3 h / 200 °C / Inert atmosphere

2: potassium hydroxide / methanol / 2.5 h / Reflux

3: N-Bromosuccinimide / acetonitrile / 8 h / 20 °C

With N-Bromosuccinimide; potassium hydroxide; In methanol; acetonitrile;
DOI:10.1039/c5cc05390k