3,4-Dichlorobenzyl dimethylcarbamodithioate

Base Information

• Chemical Name: 3,4-Dichlorobenzyl dimethylcarbamodithioate
• CAS No.: 29023-36-7
• Molecular Formula: C10H11Cl2NS2
• Molecular Weight: 280.242
• Hs Code.: 2930909090
• NSC Number: 24914
• DSSTox Substance ID: DTXSID80282201
• Wikidata: Q82016415
• Mol file: 29023-36-7.mol

Synonyms:29023-36-7;3,4-dichlorobenzyl dimethylcarbamodithioate;NSC24914;DTXSID80282201;NSC-24914

Chemical Property of 3,4-Dichlorobenzyl dimethylcarbamodithioate

Chemical Property:

• Vapor Pressure: 2.38E-05mmHg at 25°C
• Boiling Point: 359.4°Cat760mmHg
• Flash Point: 171.2°C
• PSA: 60.63000
• Density: 1.364g/cm³
• LogP: 4.07310
• XLogP3: 4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 278.9709971
• Heavy Atom Count: 15
• Complexity: 224

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN(C)C(=S)SCC1=CC(=C(C=C1)Cl)Cl

Technology Process of 3,4-Dichlorobenzyl dimethylcarbamodithioate

There total 1 articles about 3,4-Dichlorobenzyl dimethylcarbamodithioate 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:

3,4-Dichlorophenylmethyl chloride (102-47-6) + Oxo-phenylamino-acetyl azide → dimethyl-dithiocarbamic acid-(3,4-dichloro-benzyl ester) (29023-36-7)

Guidance literature:

With acetone;

DOI:10.1139/v56-142

Reference yield:

dimethyl-dithiocarbamic acid-(3,4-dichloro-benzyl ester) (29023-36-7) → 3,4-dichlorobenzyl mercaptan (36480-40-7)

Guidance literature:

With sodium hydroxide;

DOI:10.1139/v56-142

upstream raw materials:

3,4-Dichlorophenylmethyl chloride

Downstream raw materials:

3,4-dichlorobenzyl mercaptan