2,4-Dibromobenzenethiol

Base Information

• Chemical Name: 2,4-Dibromobenzenethiol
• CAS No.: 70009-86-8
• Molecular Formula: C6H4Br2S
• Molecular Weight: 267.972
• DSSTox Substance ID: DTXSID90577377
• Wikidata: Q82467347
• Mol file: 70009-86-8.mol

Synonyms:2,4-Dibromobenzenethiol;70009-86-8;2,4-Dibromobenzene-1-thiol;Benzenethiol, 2,4-dibromo-;2,4-dibromothiophenol;2,4-Dibromo-benZenethiol;SCHEMBL4304179;DTXSID90577377;MFCD00068900;EN300-673702

Chemical Property of 2,4-Dibromobenzenethiol

Chemical Property:

• XLogP3: 3.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 267.83800
• Heavy Atom Count: 9
• Complexity: 97.1

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1Br)Br)S

Technology Process of 2,4-Dibromobenzenethiol

There total 1 articles about 2,4-Dibromobenzenethiol 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:

2,4-dibromo-aniline (615-57-6) → 2,4-dibromothiophenol (70009-86-8)

Guidance literature:

Reference yield: 76.2%

2,4-dibromo-1-fluorobenzene (1435-53-6) + 2,4-dibromothiophenol (70009-86-8) → C12H6Br4S

Guidance literature:

With potassium carbonate; In dimethyl sulfoxide; at 110 ℃; for 8h; Inert atmosphere;

Reference yield:

2,4-dibromothiophenol (70009-86-8) + 2-bromobenzanilide (10282-57-2) → C19H13Br2NOS

Guidance literature:

With copper(l) iodide; potassium tert-butylate; N,N`-dimethylethylenediamine; In N,N-dimethyl-formamide; at 100 ℃; for 12h; Reagent/catalyst; chemoselective reaction; Inert atmosphere; Schlenk technique;

DOI:10.1055/s-0036-1558959

upstream raw materials:

2,4-dibromo-aniline

Downstream raw materials:

bis-(2,4-dibromo-phenyl)-disulfide

2,4-dibromophenyl-thioacetic acid

2,4-dibromophenyl-sulfonylacetic acid

2,4-dibromophenyl-sulfinylacetic acid