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经验公式(希尔记法):
C8H7NO2
化学文摘社编号:
分子量:
149.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
113290
Assay:
99%
Form:
solid
InChI key
VUVORVXMOLQFMO-ONEGZZNKSA-N
SMILES string
[H]\C(=C(\[H])c1cccnc1)C(O)=O
InChI
1S/C8H7NO2/c10-8(11)4-3-7-2-1-5-9-6-7/h1-6H,(H,10,11)/b4-3+
assay
99%
form
solid
mp
232-235 °C (dec.) (lit.)
Quality Level
General description
trans-3-(3-Pyridyl)acrylic acid, a bifunctional ligand with both hard and soft coordination sites, is mainly used in constructing heterometallic complexes.
Application
trans-3-(3-Pyridyl)acrylic acid has been used as an organic linker to connect d and f block metals to form a 3D heterometallic coordination polymer with luminescence property. It may also be used in the synthesis of ethyl trans-3-(3-pyridyl)acrylate via esterification.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Combination of covalent and hydrogen bonding in the formation of 3D uranyl-carboxylate networks.
Dalai S
Inorgorganica Chimica Acta, 363(13), 3407-3412 (2010)
Interparticle spacing control in the superlattices of carboxylic acid-capped gold nanoparticles by hydrogen-bonding mediation.
Yao H
Langmuir, 20(23), 10317-10323 (2004)
Assembling metals (Co II and Mn II) with pyridylcarboxylates in the presence of azide: synthesis, structural aspects and magnetic behavior of three coordination polymers.
Mondal K
Dalton Transactions, 6, 767-775 (2008)
Novel coordination polymers and structural systematics in the hydrothermal M, M? trans-3 (-3-pyridyl) acrylic acid system.
Gunning N
Dalton Transactions, 16, 2788-2792 (2005)
Uranyl Ion Complexes with trans?3?(3?Pyridyl) acrylic Acid Including a Uranyl?Copper (II) Heterometallic Framework.
Thuery P
European Journal of Inorganic Chemistry, 2014(28), 4772-4778 (2014)
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