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Merck
CN

123080

2-氨基-4-甲基吡啶

99%

别名:

2-氨基-4-甲基吡啶

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关于此项目

经验公式(希尔记法):
C6H8N2
化学文摘社编号:
分子量:
108.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-780-9
Beilstein/REAXYS Number:
107066
MDL number:
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产品名称

2-氨基-4-甲基吡啶, 99%

InChI key

ORLGLBZRQYOWNA-UHFFFAOYSA-N

InChI

1S/C6H8N2/c1-5-2-3-8-6(7)4-5/h2-4H,1H3,(H2,7,8)

SMILES string

Cc1ccnc(N)c1

assay

99%

bp

230 °C (lit.)

mp

96-99 °C (lit.)

solubility

DMF: freely soluble
H2O: freely soluble
aliphatic hydrocarbons: slightly soluble
coal tar bases: freely soluble
lower alcohols: freely soluble
petroleum ether: slightly soluble

Quality Level

Gene Information

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Biochem/physiol Actions

2-氨基-4-甲基吡啶抑制体外 小鼠 RAW 264.7 细胞分离的诱导型 NO 合成酶的活性

General description

2-氨基-4-甲基吡啶作为配体,形成甲氧基桥联的铜 (II) 配合物

Application

2-氨基-4-甲基吡啶用于合成 2-氨基-4-甲基吡啶-2-羟基苯甲酸盐

pictograms

Skull and crossbonesCorrosion

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 2

flash_point_f

244.4 °F - closed cup

flash_point_c

118 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Somnath Ray Choudhury et al.
Dalton transactions (Cambridge, England : 2003), (37)(37), 7617-7624 (2009-09-18)
The crystal lattice of the three isostructural compounds , (C(6)H(8)N(2)H)(2)[M(C(3)H(2)O(4))(2)(H(2)O)(2)].4H(2)O (C(6)H(8)N(2)H = protonated 2-amino-4-picoline, M = Ni/Co/Mn, C(3)H(4)O(4) = malonate dianion; hereafter, malonate) is formed by supramolecular 2D layers. Hydrogen-bonding, pi...pi and lone pair...pi interactions play crucial role in organizing
Analgesic activity of 2-amino-4-methylpyridine, a novel NO synthase inhibitor.
E R Pettipher et al.
Inflammation research : official journal of the European Histamine Research Society ... [et al.], 46 Suppl 2, S135-S136 (1997-08-01)
Eun-Ae Jo et al.
Chemical communications (Cambridge, England), (44)(44), 5779-5781 (2008-11-15)
The hydroacylation of methanol with alkenes was developed using a catalytic system consisting of Rh(I), 2-amino-4-picoline and benzoic acid; the reaction is speculated to occur by the initial N-methylation of 2-amino-4-picoline with methanol, and the subsequent dehydrogenation of the resulting
Ravil R Petrov et al.
Bioorganic & medicinal chemistry letters, 16(18), 4946-4950 (2006-07-11)
An enkephalin analogue coupled to 'aminofentanyl' has been synthesized and tested for biological activities at the mu and delta opioid receptors. Aminofentanyl which represents a structural derivative of fentanyl has been synthesized by acylation of 1-(2-phenethyl)-4-(N-anilino)piperidine with phthaloyl protected beta-alaninyl
R Boer et al.
Molecular pharmacology, 58(5), 1026-1034 (2000-10-20)
We have investigated various nitric oxide (NO) synthase inhibitors for their affinity and selectivity toward the three human isoenzymes in radioligand binding experiments. Therefore, we developed the new radioligand [(3)H]2-amino-4-picoline to measure binding of these compounds to the three human

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