2,4,5-Tribromotoluene

Base Information

• Chemical Name: 2,4,5-Tribromotoluene
• CAS No.: 3278-88-4
• Molecular Formula: C7H5Br3
• Molecular Weight: 328.829
• Hs Code.: 2903999090
• European Community (EC) Number: 660-935-0
• DSSTox Substance ID: DTXSID30186447
• Wikidata: Q72509895
• Mol file: 3278-88-4.mol

Synonyms:2,4,5-Tribromotoluene;1,2,4-tribromo-5-methylbenzene;3278-88-4;Benzene, 1,2,4-tribromo-5-methyl-;MFCD00052984;2,4,5-Tribrom-toluol;SCHEMBL11045804;DTXSID30186447;KZZJNNUPNNBCCH-UHFFFAOYSA-N;AMY31924;2,4,5-Tribromotoluene, AldrichCPR;BBL100458;CK1101;STL554252;AKOS005254423;DS-17909;CS-0153311;FT-0606248;A821415

Chemical Property of 2,4,5-Tribromotoluene

Chemical Property:

• Vapor Pressure: 0.00214mmHg at 25°C
• Melting Point: 112-114 °C
• Refractive Index: 1.619
• Boiling Point: 299.3 °C at 760 mmHg
• Flash Point: 132.5 °C
• PSA: 0.00000
• Density: 2.131 g/cm³
• LogP: 4.28250
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility.: DMSO, Methanol (Slightly)
• XLogP3: 4.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 327.79209
• Heavy Atom Count: 10
• Complexity: 115

Purity/Quality:

98% or more ^*data from raw suppliers

2,4,5-Tribromotoluene ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn,T,Xi
• Hazard Codes: Xn,T,Xi

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=C(C=C1Br)Br)Br
• Uses: 2,4,5-Tribromotoluene can be used as a method for decompoising halogenated organic compounds.

Technology Process of 2,4,5-Tribromotoluene

There total 14 articles about 2,4,5-Tribromotoluene 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: 90.0%

toluene (108-88-3,15644-74-3,16713-13-6) → pentabromotoluene (87-83-2,26101-97-3) + 2,4,5-tribromotoluene (3278-88-4) + 2,3,4,5-tetrabromotoluene (101421-20-9)

Guidance literature:

With bromine; Nitrogen dioxide; In water; trifluoroacetic acid; at 20 ℃; for 0.1h; Product distribution; other time;

Reference yield:

tetrachloromethane (56-23-5) + 2,4-dibromotoluene (31543-75-6) + bromine (7726-95-6) → 2,4,5-tribromotoluene (3278-88-4) + 2,4,6-tribromotoluene (6320-40-7)

Guidance literature:

Reference yield:

para-bromotoluene (106-38-7) → 3,4-dibromotoluene (60956-23-2) + 2,4-dibromotoluene (31543-75-6) + 2,4,5-tribromotoluene (3278-88-4)

Guidance literature:

beim Bromieren;

upstream raw materials:

1,4-dibromo-2-methylbenzene

para-bromotoluene

3,4-dibromotoluene

2,4-dibromotoluene

Downstream raw materials:

2,4,5-tribromo-benzoic acid

Refernces