6-Bromo-1,8-naphthyridin-2-ol - CAS 72754-05-3

Catalog:	BB034682
Product Name:	6-Bromo-1,8-naphthyridin-2-ol
CAS:	72754-05-3
Synonyms:	6-bromo-1H-1,8-naphthyridin-2-one

Technical Data

Patents

Computed Properties

IUPAC Name:	6-bromo-1H-1,8-naphthyridin-2-one
Description:	6-Bromo-1,8-naphthyridin-2-ol (CAS# 72754-05-3) is a useful research chemical.
Molecular Weight:	225.04
Molecular Formula:	C8H5BrN2O
Canonical SMILES:	C1=CC(=O)NC2=NC=C(C=C21)Br
InChI:	InChI=1S/C8H5BrN2O/c9-6-3-5-1-2-7(12)11-8(5)10-4-6/h1-4H,(H,10,11,12)
InChI Key:	BCEWGGGNOQNYKK-UHFFFAOYSA-N
Boiling Point:	415.941 °C at 760 mmHg
Purity:	95 %
Density:	1.711 g/cm³
Appearance:	Light brown powder
MDL:	MFCD07781151
LogP:	2.09790

Publication Number	Title	Priority Date
AU-2016371387-A1	Tricyclic compounds and compositions as kinase inhibitors	20151218
CA-3008098-A1	Tricyclic compounds and compositions as kinase inhibitors	20151218
EP-3390404-A1	Tricyclic compounds and compositions as kinase inhibitors	20151218
JP-2018537508-A	Tricyclic compounds and compositions as kinase inhibitors	20151218
KR-20180095595-A	Tricyclic compounds and compositions as kinase inhibitors	20151218

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Related Functional Groups

Naphthyridines

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(R)-4-((R)-1-((7-(3,4,5-Trimethoxyphenyl)-1,6-naphthyridin-5-yl)oxy)ethyl)pyrrolidin-2-one
[127094-58-0]
Ethyl 6-chloro-4-hydroxy[1,5]naphthyridine-3-carboxylate
[64436-97-1]
Ethyl 7-Bromo-4-hydroxy-1,5-naphthyridine-3-carboxylate
[40499-89-6]
2,7-naphthyridine-4-carboxylic acid
[1303588-27-3]
7-Chloro-1,2,3,4-tetrahydro-1,8-naphthyridine
[28252-82-6]
2,4-Dichloro-1,5-naphthyridine

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Complexity:	229
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	223.95853
Formal Charge:	0
Heavy Atom Count:	12
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	223.95853
Rotatable Bond Count:	0
Topological Polar Surface Area:	42
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	1.3