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重要文件

A68300

Sigma-Aldrich

2-氨基吡啶-3-羧酸

98%

同義詞:

2-氨基烟酸, 2-氨基吡啶-3-羧酸

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About This Item

經驗公式(希爾表示法):
C6H6N2O2
CAS號碼:
分子量::
138.12
Beilstein:
119031
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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化驗

98%

形狀

powder

mp

295-297 °C (dec.) (lit.)

SMILES 字串

Nc1ncccc1C(O)=O

InChI

1S/C6H6N2O2/c7-5-4(6(9)10)2-1-3-8-5/h1-3H,(H2,7,8)(H,9,10)

InChI 密鑰

KPIVDNYJNOPGBE-UHFFFAOYSA-N

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應用

2-氨基吡啶-3-羧酸可用作:
  • 制备铜(II)有机配位化合物的配体。[1]
  • 通过与三甲基硅基氰化物和苯二醛反应制备吡啶并[2′,1′2,3]咪唑并[4,5-c]异喹啉的反应物。[2]
  • 合成有机可溶性、热稳定性聚(硫脲-酰胺-酰亚胺)聚合物的反应物。[3]

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Synthesis, characterization, spectroscopic and electrochemical investigation of 2-aminopyridine-3-carboxylic acid copper (II) complexes with diimine
Srivastava AK, et al.
Chemical Data Collections, 24, 100272-100272 (2019)
Mehmet Karabacak et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 91, 83-96 (2012-03-01)
The experimental (UV-vis and FT-IR) and theoretical study of 2-aminonicotinic acid (C(6)H(6)N(2)O(2)) was presented in this work. The ultraviolet absorption spectrum of title molecule that dissolved in ethanol and water were examined in the range of 200-400 nm. The FT-IR
Ronald Bartzatt
Drugs in R&D, 8(6), 363-372 (2007-10-30)
Nitrogen mustard (N-mustard) compounds are considered important anticancer drugs. Various transporting agents have been utilised to carry N-mustard groups including coumarins, amides, polyaromatic molecules and cycloalkyl structures. N-mustards act as bifunctional alkylating agents that induce cross-linking within DNA strands and
Novel thermally stable poly (thiourea-amide-imide) s bearing CS moieties and pyridine units in the backbone: Synthesis and properties
Kausar A, et al.
Polymer Degradation and Stability, 95(12), 2611-2618 (2010)
Synthesis of pyrido [2′, 1′: 2, 3] imidazo [4, 5-c] isoquinolines via a one-pot, three-component reaction
Maleki A and Rezayan AH
Tetrahedron Letters, 55(10), 1848-1850 (2014)

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