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Details

Stereochemistry ACHIRAL
Molecular Formula C4H8Br2
Molecular Weight 215.914
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,4-DIBROMOBUTANE

SMILES

BrCCCCBr

InChI

InChIKey=ULTHEAFYOOPTTB-UHFFFAOYSA-N
InChI=1S/C4H8Br2/c5-3-1-2-4-6/h1-4H2

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparison of electrospray ionization, atmospheric pressure photoionization, and anion attachment atmospheric pressure photoionization for the analysis of hexabromocyclododecane enantiomers in environmental samples.
2010-12-10
Polyamine aza-cyclic compounds demonstrate anti-proliferative activity in vitro but fail to control tumour growth in vivo.
2010-11
5,5'-Diphenyl-2,2'-[butane-1,4-diylbis(sulfanedi-yl)]bis-(1,3,4-oxadiazole).
2010-10-23
3,3'-Dimethyl-1,1'-(butane-1,4-di-yl)diimidazolium bis-(tetra-fluoro-borate).
2010-05-08
4'-Bromo-butyl ent-16-oxobeyeran-19-oate.
2010-02-13
Lesions in the Larynx of Wistar RccHan: WIST Rats.
2009-12
Synthesis, pharmacological and antiviral activity of 1,3-thiazepine derivatives.
2009-12
1,4-Bis(2-nitro-phen-oxy)butane.
2009-11-25
Kinetics of core-shell nanoparticle formation by two-dimensional nuclear magnetic resonance.
2009-06-02
Synthesis, Antiinflammatory and HIV-1 Integrase Inhibitory Activities of 1,2-Bis[5-thiazolyl]ethane-1,2-dione Derivatives.
2009-05
Poly[[[diaqua-cobalt(II)]-bis-[μ-1,1'-(butane-1,4-di-yl)diimidazole-κN:N]] dichloride tetra-hydrate].
2009-03-06
Poly[[[diaqua-cobalt(II)]-bis-[μ(2)-1,1'-(butane-1,4-di-yl)diimidazole-κN:N]] dinitrate].
2009-02-25
(Cyclo-pentane-1,1-di-yl)dimethanol.
2009-02-06
2,2'-(Butane-1,4-di-yl)diisoquinolinium tetra-chloridozincate(II).
2008-11-26
catena-Poly[[[diaqua-copper(II)]-bis-[μ-1,1'-(butane-1,4-di-yl)diimidazole-κN:N]] dinitrate].
2008-08-30
3,3'-(Butane-1,4-di-yl)diimidazole-1,1'-diium bis-(triiodide).
2008-07-19
1,1'-(Butane-1,4-diyl)di-1H-imidazole-benzene-1,3,5-triol-water (1/1/1).
2008-07-19
1,1'-(Butane-1,4-di-yl)diimidazole-3,3'-diium tetra-chloridozincate(II) dihydrate.
2008-04-04
1,1'-Dimethyl-1,1'-(butane-1,4-di-yl)dipyrrolidinium dibromide methanol disolvate.
2008-01-11
Controlled chemical stabilization of self-assembled PS-P4VP nanostructures.
2008-01-01
Covalent attachment of the plant natural product naringenin to small glass and ceramic beads.
2005-10-10
Synthesis of new hexahydro- and octahydropyrido[1,2-c]pyrimidine derivatives with an arylpiperazine moiety as ligands for 5-HT1A and 5-HT2A receptors. Part III.
2004-10-21
Chromatographic molecular recognition for catechol-related compounds using thiacalix[4]arene as an effective selector.
2004-09
Chiral polymers containing a carbohydrate moiety: synthesis.
2004-04-19
[Study on the synthesis and spectra of 2-thenoyl-2-carbazolyl-N-butyltrifluoroacetone].
2004-02
Synthesis of new hexahydro- and octahydropyrido[1,2-c]pyrimidine derivatives with an arylpiperazine moiety as ligands for 5-HT(1A) and 5-HT(2A) receptors, Part 2.
2004-02
Metabolism and mutagenicity of source water contaminants 1,3-dichloropropane and 2,2-dichloropropane.
2004-01
Bridged tetraquaternary salts from N,N'-polyfluoroalkyl-4,4'-bipyridine.
2003-11-17
The synthesis of carboacycles derived from B,B'-bis(aryl) derivatives of icosahedral ortho-carborane.
2003-06-16
Synthesis of new hexahydro- and octahydropyrido[1,2-c]pyrimidine derivatives with an arylpiperazine moiety as ligands for 5-HT1A and 5-HT2A receptors.
2002-12
Synthesis of 1,4-disubstituted 2-methylpiperazine derivatives, new 5-HT(1A) receptor ligands.
2002-03-06
Preparation of new nitrogen-bridged heterocycles. 51. Syntheses and structures of compounds having two indolizine nuclei in a molecule.
2001-11
Extraction of metal ions using chemically modified silica gel: a PIXE analysis.
2001-08-30
Patents
Name Type Language
NSC-71435
Preferred Name English
1,4-DIBROMOBUTANE
Systematic Name English
DIBROMOBUTANE, 1,4-
Systematic Name English
Code System Code Type Description
NSC
71435
Created by admin on Mon Mar 31 18:52:22 GMT 2025 , Edited by admin on Mon Mar 31 18:52:22 GMT 2025
PRIMARY
PUBCHEM
8056
Created by admin on Mon Mar 31 18:52:22 GMT 2025 , Edited by admin on Mon Mar 31 18:52:22 GMT 2025
PRIMARY
FDA UNII
G49PHR6JFU
Created by admin on Mon Mar 31 18:52:22 GMT 2025 , Edited by admin on Mon Mar 31 18:52:22 GMT 2025
PRIMARY
MESH
C050754
Created by admin on Mon Mar 31 18:52:22 GMT 2025 , Edited by admin on Mon Mar 31 18:52:22 GMT 2025
PRIMARY
CAS
110-52-1
Created by admin on Mon Mar 31 18:52:22 GMT 2025 , Edited by admin on Mon Mar 31 18:52:22 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-775-5
Created by admin on Mon Mar 31 18:52:22 GMT 2025 , Edited by admin on Mon Mar 31 18:52:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID5044364
Created by admin on Mon Mar 31 18:52:22 GMT 2025 , Edited by admin on Mon Mar 31 18:52:22 GMT 2025
PRIMARY