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A78608

Sigma-Aldrich

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
Beilstein:
107014
EC Number:
203-648-4
MDL number:
MFCD00006089
UNSPSC Code:
12352100
PubChem Substance ID:
24891286
NACRES:
NA.22

Quality Level

100

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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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

A78608-5KG:
A78608-500G:
A78608-100G:
A78608-VAR:
A78608-5G:
A78608-10KG:
A78608-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
STBL2756
STBK9755
STBK2683
STBK0349
STBK0350

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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
Manuel Tzouros et al.
Chemical research in toxicology, 22(5), 853-862 (2009-03-26)
Covalent binding of reactive metabolites is generally accepted as one underlying mechanism of drug-induced toxicity. However, identification of protein targets by reactive metabolites still remains a challenge due to their low abundance. Here, we report the development of a highly
Robert J Altenbach et al.
Journal of medicinal chemistry, 51(20), 6571-6580 (2008-09-25)
A series of 2-aminopyrimidines was synthesized as ligands of the histamine H4 receptor (H4R). Working in part from a pyrimidine hit that was identified in an HTS campaign, SAR studies were carried out to optimize the potency, which led to
View All Related Papers

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