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方案
97%
表单
powder
mp
122-126 °C (lit.)
SMILES字符串
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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此商品 | A77997 | V900286 | 736023 |
|---|---|---|---|
| Quality Level 100 | Quality Level 100 | Quality Level - | Quality Level 100 |
| mp 122-126 °C (lit.) | mp 54-58 °C (lit.) | mp 122-126 °C (lit.) | mp 65-70 °C |
| form powder | form crystals | form - | form solid |
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
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
Manishkumar D Joshi et al.
Journal of chromatography. A, 1308, 161-165 (2013-08-21)
A reversed-phase high performance liquid chromatography (HPLC) method is described for the determination of boronic acids that are commonly present as impurities in pinacolboronate ester reagents. Boronic acids and their pinacolboronate esters are key reagents in the Suzuki-Miyaura coupling reaction.
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
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