Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

1,4-Dibromobutane

Base Information
  • Chemical Name:1,4-Dibromobutane
  • CAS No.:110-52-1
  • Deprecated CAS:625084-39-1
  • Molecular Formula:C4H8Br2
  • Molecular Weight:215.916
  • Hs Code.:29033036
  • European Community (EC) Number:203-775-5
  • NSC Number:71435
  • UNII:G49PHR6JFU
  • DSSTox Substance ID:DTXSID5044364
  • Nikkaji Number:J372G
  • Wikidata:Q161522
  • ChEMBL ID:CHEMBL3185714
  • Mol file:110-52-1.mol
1,4-Dibromobutane

Synonyms:1,4-dibromobutane

Suppliers and Price of 1,4-Dibromobutane
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-Dibromobutane
  • 500g
  • $ 250.00
  • TCI Chemical
  • 1,4-Dibromobutane >98.0%(GC)
  • 25g
  • $ 18.00
  • TCI Chemical
  • 1,4-Dibromobutane >98.0%(GC)
  • 500g
  • $ 75.00
  • Sigma-Aldrich
  • 1,4-Dibromobutane 99%
  • 500g
  • $ 87.90
  • Sigma-Aldrich
  • 1,4-Dibromobutane for synthesis. CAS 110-52-1, chemical formula Br(CH ) Br., for synthesis
  • 8032750250
  • $ 96.20
  • Sigma-Aldrich
  • 1,4-Dibromobutane 99%
  • 100g
  • $ 26.80
  • Oakwood
  • 1,4-Dibromobutane
  • 5g
  • $ 10.00
  • Oakwood
  • 1,4-Dibromobutane
  • 1g
  • $ 9.00
  • Oakwood
  • 1,4-Dibromobutane
  • 25g
  • $ 13.00
  • Oakwood
  • 1,4-Dibromobutane
  • 100g
  • $ 18.00
Total 224 raw suppliers
Chemical Property of 1,4-Dibromobutane
Chemical Property:
  • Appearance/Colour:Clear, colorless liquid 
  • Vapor Pressure:0.544mmHg at 25°C 
  • Melting Point:- 20 °C(lit.) 
  • Refractive Index:n20/D 1.519(lit.)  
  • Boiling Point:197 °C at 760 mmHg 
  • Flash Point:65.2 °C 
  • PSA:0.00000 
  • Density:1.785 g/cm3 
  • LogP:2.55640 
  • Storage Temp.:Store below +30°C. 
  • Solubility.:0.35g/l 
  • Water Solubility.:immiscible 
  • XLogP3:2.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:3
  • Exact Mass:215.89723
  • Heavy Atom Count:6
  • Complexity:17.5
Purity/Quality:

99% *data from raw suppliers

1,4-Dibromobutane *data from reagent suppliers

Safty Information:
  • Pictogram(s): ToxicT,IrritantXi,Corrosive
  • Hazard Codes:T,Xi,C 
  • Statements: 25-37/38-41-36/37/38 
  • Safety Statements: 26-39-45-37/39 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Other Classes -> Halogenated Aliphatics, Saturated
  • Canonical SMILES:C(CCBr)CBr
  • Uses 1,4-Dibromo butane was used to investigate the metabolism of two halopropanes: 1,3-dichloropropane and 2,2-dichloropropane. It was used as reagent during the synthesis of diazadioxa oxovanadium(IV) macrocyclic complexes. 1,4-Dibromobutane is used as an intermediate involved in the synthesis of active pharmaceutical ingredient and other organic compounds. It is also used in the investigation of metabolism of two halopropanes such as 1,3-dichloropropane and 2,2-dichloropropane. Further, it acts as a reagent to prepare diazadioxa oxovanadium(IV) macrocyclic complexes.
Technology Process of 1,4-Dibromobutane

There total 48 articles about 1,4-Dibromobutane 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:
Guidance literature:
With 1,2-dibromo-1,1,2,2-tetrachloroethane; triphenylphosphine; In dichloromethane; at 20 ℃; for 0.15h;
DOI:10.3906/kim-1804-41
Guidance literature:
With water; boron tribromide; In dichloromethane; at 23 ℃; for 23h; regioselective reaction;
DOI:10.1039/d0sc02567d
Guidance literature:
With sulfuric acid; sodium bromide; In water; for 3h; Heating;
Refernces

Synthesis of analogues of the calicheamicin γ1(I) oligosaccharide as potential DNA ligands

10.1016/S0040-4039(98)02135-2

The research aimed to chemically synthesize two analogues of the calicheamicin oligosaccharide, which is crucial for drug-DNA interaction and the selectivity and specificity of DNA cleavage. The study focused on the roles of carbohydrate rings D and E, the aromatic ring-C, and the β-N-O glycosidic bond on DNA-drug recognition events. The researchers reported the total synthesis of oligosaccharides 1 and 2, which replaced carbohydrate ring E with a basic chain E', either with or without the rhamnopyranosyl unit D. Key chemicals used in the synthesis process included 2,2,2-trifluoroethanesulfonyl chloride, benzoyl chloride, trifluoroethanesulfonate ester, 1,4-dibromobutane, sodium hydride, ethylamine, Fmoc-protected amine, sodium borohydride, boron trifluoride, and various other reagents and solvents. The synthesized oligosaccharides showed some binding to double-stranded DNA, but solubility issues prevented a detailed study. The work was financially supported by the Ministère de l'Enseignement Supérieur et de la Recherche and involved collaboration with experts in the field.

Synthesis, crystal structure and photophysical properties of a novel Pt(II) complex with multi-functionalized cyclometalating ligand

10.1016/j.inoche.2010.02.016

The study focuses on the synthesis, crystal structure, and photophysical properties of a novel Pt(II) complex with a multi-functionalized cyclometalating ligand. The complex, [(L)PtCl] (HL=4-{p-[N-(4-(9-carbazole))butyl-N-phenyl]aniline}-6-phenyl-2,2′-bipyridine), was synthesized using various chemicals including carbazole, 1,4-dibromobutane, 4-(p-bromophenyl)-6-phenyl-2,2′-bipyridine, aniline, and K2PtCl4. The ligand HL was designed to integrate a carbazole unit and an arylamine-modified [(C^N^N)PtCl] emissive center, aiming to simplify the production process of OLEDs and study the interaction between these components. The crystal structure of the complex was determined by X-ray crystallography, revealing a distorted square planar configuration around the Pt atom and a 2D lamellar packing system. The complex exhibits strong metal-to-ligand charge transfer (1MLCT) transitions and phosphorescence, with an intramolecular energy transfer process from the carbazole unit to the emissive center. The study also includes the absorption and emission spectra of the ligand and complex, highlighting their potential applications in organic light-emitting diodes.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 110-52-1