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A78608

Sigma-Aldrich

2-Aminopyrimidine

97%

Sinónimos:

2-Pyrimidinamine

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About This Item

Fórmula empírica (notación de Hill):
C4H5N3
Número de CAS:
109-12-6
Peso molecular:
95.10
Beilstein/REAXYS Number:
107014
EC Number:
203-648-4
MDL number:
MFCD00006089
UNSPSC Code:
12352100
PubChem Substance ID:
24891286
NACRES:
NA.22

assay

97%

form

powder

mp

122-126 °C (lit.)

SMILES string

Nc1ncccn1

InChI

1S/C4H5N3/c5-4-6-2-1-3-7-4/h1-3H,(H2,5,6,7)

InChI key

LJXQPZWIHJMPQQ-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Sigma-Aldrich

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Sigma-Aldrich

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D S Ermolat'ev et al.
Molecular diversity, 15(2), 491-496 (2010-08-27)
An efficient microwave-assisted one-pot two-step protocol was developed for the construction of disubstituted 2-amino-1H-imidazoles. This process involves the sequential formation of 2,3-dihydro-2-hydroxyimidazo[1,2-a]pyrimidinium salts from readily available 2-aminopyrimidines and α-bromoketones, followed by cleavage of the pyrimidine ring with hydrazine.
S A Abdel-Latif et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 67(3-4), 950-957 (2006-11-07)
The formation constants of some transition metal ions Cr(III), Mn(II), Fe(III), Ni(II) and Cu(II) binary complexes containing Schiff bases resulting from condensation of salicylaldehyde with aniline (I), 2-aminopyridine (II), 4-aminopyridine (III) and 2-aminopyrimidine (IV) were determined pH-metrically in ethanolic medium
Rogier A Smits et al.
Drug discovery today, 14(15-16), 745-753 (2009-05-30)
The search for new and potent histamine H4 receptor ligands is leading to a steadily increasing number of scientific publications and patent applications. Several interesting and structurally diverse compounds have been found, but fierce IP competition for a preferred 2-aminopyrimidine
Nimisha Singh et al.
Bioorganic & medicinal chemistry letters, 21(15), 4404-4408 (2011-07-09)
An economical and efficient one step synthesis of a series of 8-(arylidene)-4-(aryl)-5,6,7,8-tetrahydro-quinazolin-2-ylamines and 9-(arylidene)-4-(aryl)-6,7,8,9-tetrahydro-5H-cycloheptapyrimidin-2-ylamines by the reaction of bis-benzylidene cycloalkanones and guanidine hydrochloride in presence of NaH has been developed. All the synthesized compounds were evaluated against Mycobacterium tuberculosis H(37)Rv
Kamaljit Singh et al.
European journal of medicinal chemistry, 52, 82-97 (2012-03-31)
2-Aminopyrimidine based 4-aminoquinolines were synthesized using an efficacious protocol. Some of the compounds showed in vitro anti-plasmodial activity against drug-sensitive CQ(S) (3D7) and drug-resistant CQ(R) (K1) strains of Plasmodium falciparum in the nM range. In particular, 5-isopropyloxycarbonyl-6-methyl-4-(2-nitrophenyl)-2-[(7-chloroquinolin-4-ylamino)butylamino] pyrimidine depicted the lowest
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