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5-Acetyl-4-Chloro-7H-pyrrolo[2,3-d]pyrimidine

5-Acetyl-4-Chloro-7H-pyrrolo[2,3-d]pyrimidine - CAS 1363381-59-2

Catalog:	BB008344
Product Name:	5-Acetyl-4-Chloro-7H-pyrrolo[2,3-d]pyrimidine
CAS:	1363381-59-2
Synonyms:	1-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethanone; 1-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethanone

Technical Data

Patents

Computed Properties

IUPAC Name:	1-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethanone
Description:	5-Acetyl-4-Chloro-7H-pyrrolo[2,3-d]pyrimidine (CAS# 1363381-59-2 ) is a useful research chemical.
Molecular Weight:	195.61
Molecular Formula:	C8H6ClN3O
Canonical SMILES:	CC(=O)C1=CNC2=C1C(=NC=N2)Cl
InChI:	InChI=1S/C8H6ClN3O/c1-4(13)5-2-10-8-6(5)7(9)11-3-12-8/h2-3H,1H3,(H,10,11,12)
InChI Key:	KXOFBMPFLUKIJL-UHFFFAOYSA-N
LogP:	1.81390

Publication Number	Title	Priority Date
US-2016101188-A1	Novel nanocarrier delivered cancer chemotherapeutic agents	20130531
PT-2132216-E	INNOVATIVE ANALOGS OF NUCLEOIDS FOR THE TREATMENT OF VIRAL INFECTIONS	20070209
US-2005124623-A1	Diazaindole-dicarbonyl-piperazinyl antiviral agents	20031126
US-2008125439-A1	Diazaindole-dicarbonyl-piperazinyl antiviral agents	20031126
US-7902204-B2	Diazaindole-dicarbonyl-piperazinyl antiviral agents	20031126

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Related Functional Groups

Carbonyl Compounds

[91125-43-8]
Sulfophenyl nonanoate sodium salt
[5650-34-0]
Oxiran-2-yl(phenyl)methanone
[959574-98-2]
(3-Phenyl-1H-pyrazol-1-yl)acetic acid
[35153-16-3]
(Z)-10-Tetradecenyl Acetate
[832741-29-4]
1-(4-Bromo-5-propylthiophen-2-yl)ethanone
[253429-30-0]
1-Bromo-2-(2,2-diethoxyethoxy)-4-fluorobenzene

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Complexity:	223
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	195.0199395
Formal Charge:	0
Heavy Atom Count:	13
Hydrogen Bond Acceptor Count:	3
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	195.0199395
Rotatable Bond Count:	1
Topological Polar Surface Area:	58.6
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	1.3