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MilliporeSigma

A78608

2-Aminopyrimidine

97%

Synonym(s):

2-Pyrimidinamine

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About This Item

Empirical Formula (Hill Notation):
C4H5N3
CAS Number:
109-12-6
Molecular Weight:
95.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24891286
EC Number:
203-648-4
Beilstein/REAXYS Number:
107014
MDL number:
MFCD00006089

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Product Name

2-Aminopyrimidine, 97%

InChI key

LJXQPZWIHJMPQQ-UHFFFAOYSA-N

InChI

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

SMILES string

Nc1ncccn1

assay

97%

form

powder

mp

122-126 °C (lit.)

Quality Level

100

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2-Aminopyrimidine 97%

Sigma-Aldrich

A78608

2-Aminopyrimidine

2-Aminopyridine 99%

Sigma-Aldrich

A77997

2-Aminopyridine

3-Amino-4-iodopyridine 97%

Sigma-Aldrich

736023

3-Amino-4-iodopyridine

3-Aminopyridine 99%

Sigma-Aldrich

A78209

3-Aminopyridine

assay

97%

assay

99%

assay

97%

assay

99%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

-

form

powder

form

crystals

form

solid

form

flakes

mp

122-126 °C (lit.)

mp

54-58 °C (lit.)

mp

65-70 °C

mp

60-63 °C (lit.)

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB2627
STBL2756
STBK9755
STBK2683
STBK0349

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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.
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
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
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
Teodor Silviu Balaban et al.
Journal of the American Chemical Society, 125(14), 4233-4239 (2003-04-03)
The 2-aminopyrimidin-5-yl ligand is revealed to be a promising candidate for the construction of supramolecular porphyrin arrays with broad absorption bands for efficient light-harvesting. 10-Mono- and 10,20-di(2-aminopyrimidin-5-yl) derivatives of 5,15-bis(3,5-di-tert-butylphenyl)porphyrin have been synthesized in high yield. Their Zn(II) salts show
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