2-Aminopyrimidin-4-ol - CAS 100643-25-2

Catalog:	BB054985
Product Name:	2-Aminopyrimidin-4-ol
CAS:	100643-25-2
Synonyms:	C4H5N3O

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

Related CAS:	108-53-2
IUPAC Name:	2-amino-1H-pyrimidin-6-one
Description:	2-Aminopyrimidin-4-ol (cas# 100643-25-2) is a useful research chemical.
Molecular Weight:	111.1
Molecular Formula:	C4H5N3O
Canonical SMILES:	C1=CN=C(NC1=O)N
InChI:	InChI=1S/C4H5N3O/c5-4-6-2-1-3(8)7-4/h1-2H,(H3,5,6,7,8)
InChI Key:	XQCZBXHVTFVIFE-UHFFFAOYSA-N

Publication Number	Title	Priority Date
CN-114160171-A	CeO2-La3+Preparation method of/BiOI composite material and method for removing sulfadiazine in water	20211110
CN-113908292-A	Target-mediated nucleic acid nano preparation and preparation method thereof	20211013
CN-113698634-A	Method for preparing self-adaptive forming polymer device and application	20210713
CN-113214166-A	Synthesis process, intermediate and pharmaceutical process of 2,4, 5-triamino-6-hydroxypyrimidine	20210623
US-11220707-B1	Compositions and methods for pairwise sequencing	20210617
US-11236388-B1	Compositions and methods for pairwise sequencing	20210617
CN-113234077-A	Synthesis method of 2-amino-6-chloroguanine	20210511
CN-113234077-B	Synthesis method of 2-amino-6-chloropurine	20210511
CN-113362890-A	Method for evaluating organic matter degradation potential of biological filter material	20210428
CN-113151196-A	Recombinant vaccinia virus, vaccinia virus vector vaccine, application and preparation method thereof	20210203

PMID	Publication Date	Title	Journal
23122864	20121215	Isocytosine-based inhibitors of xanthine oxidase: design, synthesis, SAR, PK and in vivo efficacy in rat model of hyperuricemia	Bioorganic & medicinal chemistry letters
22722325	20120928	Understanding the role of base stacking in nucleic acids. MD and QM analysis of tandem GA base pairs in RNA duplexes	Physical chemistry chemical physics : PCCP
22483591	20120501	Identification of novel isocytosine derivatives as xanthine oxidase inhibitors from a set of virtual screening hits	Bioorganic & medicinal chemistry
21769372	20110907	Ditopic triply hydrogen-bonded heterodimers	Organic & biomolecular chemistry
21591661	20110707	Comprehensive core-level study of the effects of isomerism, halogenation, and methylation on the tautomeric equilibrium of cytosine	The journal of physical chemistry. A
21545144	20110607	Three-dimensional structure and catalytic mechanism of cytosine deaminase	Biochemistry
20976264	20100926	Error-Prone Translesion DNA Synthesis by Escherichia coli DNA Polymerase IV (DinB) on Templates Containing 1,2-dihydro-2-oxoadenine	Journal of nucleic acids
20665014	20100801	The role of the formamide/zirconia system in the synthesis of nucleobases and biogenic carboxylic acid derivatives	Journal of molecular evolution
20598146	20100702	Incorporation of non-natural nucleotides into template-switching oligonucleotides reduces background and improves cDNA synthesis from very small RNA samples	BMC genomics
20408056	20100301	Design and synthesis of novel SATE derivatives of acyclic isocytosine and 9-deazaadenine C-nucleosides	Nucleosides, nucleotides & nucleic acids

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GHS Hazard Statement:	H302 (97.56%): Harmful if swallowed [Warning Acute toxicity, oral]
Precautionary Statement:	P264, P264+P265, P270, P280, P301+P317, P305+P351+P338, P330, P337+P317, and P501
Signal Word:	Warning

Complexity:	170
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	111.043261792
Formal Charge:	0
Heavy Atom Count:	8
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	111.043261792
Rotatable Bond Count:	0
Topological Polar Surface Area:	67.5Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	-1