Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	54975
Common Name:	(4-bromophenyl)thiourea
Systematic Name:	1-(4-bromophenyl)thiourea
RefMet Name:	4-Bromophenylthiourea
Synonyms:	(4-bromophenyl)thiourea; 1-(p-bromophenyl)-2-thiourea; 4-Bromophenylthiourea; 4-bromophenyl thiourea; N-p-Bromophenylthiourea; p-bromophenylthiourea [PubChem Synonyms]
Exact Mass:	229.9513 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C7H7BrN2S
InChIKey:	MRVQULNOKCOGHC-UHFFFAOYSA-N
ClassyFire superclass:	Benzenoids [C0002448]
ClassyFire class:	Benzene and substituted derivatives [C0002279]
ClassyFire subclass:	N-phenylthioureas [C0002980]
ClassyFire direct parent:	N-phenylthioureas [C0002980]
SMILES:	c1cc(ccc1Br)NC(=S)N
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	2735620
CHEBI ID:	34391
KEGG ID:	C14644
Plant Metabolite Hub(Pmhub):	MS000023878

Calculated physicochemical properties (?):

Heavy Atoms:	11
Rings:	1
Aromatic Rings:	1
Rotatable Bonds:	2
van der Waals Molecular volume:	155.63 Å3 molecule-1
Toplogical Polar Sufrace Area:	38.05 Å2 molecule-1
Hydrogen Bond Donors:	2
Hydrogen Bond Acceptors:	0
logP:	2.10
Molar Refractivity:	54.55
Fraction sp3 Carbons:	0.00
sp3 Carbons:	0

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y