P51400
丙炔酸
95%
别名:
2-丙炔酸, 乙炔羧酸
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线性分子式:
HC≡CCOOH
化学文摘社编号:
分子量:
70.05
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-437-8
Beilstein/REAXYS Number:
878176
MDL number:
Assay:
95%
产品名称
丙炔酸, 95%
InChI key
UORVCLMRJXCDCP-UHFFFAOYSA-N
InChI
1S/C3H2O2/c1-2-3(4)5/h1H,(H,4,5)
SMILES string
OC(=O)C#C
assay
95%
impurities
≤6.0% acetic acid
refractive index
n20/D 1.431 (lit.)
bp
102 °C/200 mmHg (lit.)
mp
16-18 °C (lit.)
density
1.138 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
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Application
用于合成过渡金属配合物、卤烷基丙炔酸酯和卤代丙烯酸酯的试剂。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
136.4 °F - closed cup
flash_point_c
58 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Tetrahedron, 49, 4229-4229 (1993)
The Journal of Organic Chemistry, 57, 709-709 (1992)
Jihye Park et al.
The Journal of organic chemistry, 76(7), 2214-2219 (2011-03-05)
One-pot synthesis of symmetric 1,4-disubstituted 1,3-diynes from iodoarenes and propiolic acid via Sonogashira reaction followed by Pd-catalyzed decarboxylative homocoupling is developed in high yields. Also, this system allows the one-pot synthesis of unsymmetric 1,4-disubstituted 1,3-diynes by cross-coupling of two different
Wonyoung Kim et al.
Organic letters, 15(7), 1654-1657 (2013-03-15)
Diarylalkynones were synthesized from one-pot Pd-catalyzed carbonylative and noncarbonylative coupling reactions of propiolic acid with aryl iodides under a carbon monoxide atmosphere. Aryl iodide (2.0 equiv), propiolic acid (1.0 equiv), Pd(PPh3)2Cl2 (5 mol %), CuCl (10 mol %), Et3N (6.0
Dingyi Yu et al.
Proceedings of the National Academy of Sciences of the United States of America, 107(47), 20184-20189 (2010-11-10)
The use of carbon dioxide as a renewable and environmentally friendly source of carbon in organic synthesis is a highly attractive approach, but its real world applications remain a great challenge. The major obstacles for commercialization of most current protocols
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