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Merck

P51400

Sigma-Aldrich

丙炔酸

95%

别名:

2-丙炔酸, 乙炔羧酸

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About This Item

线性分子式:
HC≡CCOOH
CAS号:
分子量:
70.05
Beilstein:
878176
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

95%

雜質

≤6.0% acetic acid

折射率

n20/D 1.431 (lit.)

bp

102 °C/200 mmHg (lit.)

mp

16-18 °C (lit.)

密度

1.138 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

OC(=O)C#C

InChI

1S/C3H2O2/c1-2-3(4)5/h1H,(H,4,5)

InChI 密鑰

UORVCLMRJXCDCP-UHFFFAOYSA-N

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應用

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。

訊號詞

Danger

危險分類

Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

136.4 °F - closed cup

閃點(°C)

58 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Tetrahedron, 49, 4229-4229 (1993)
The Journal of Organic Chemistry, 57, 709-709 (1992)
Journal of Organometallic Chemistry, 456, 271-271 (1993)
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
Tina N Grant et al.
Organic letters, 10(18), 3985-3988 (2008-08-19)
Readily available five- and six-membered lactones and N-sulfonyllactams undergo efficient addition of t-butyl propiolate, and the resulting adducts undergo cycloisomerization to six- and seven-membered cyclic ethers or amines in the presence of pyridinium acetate. The ring expansion process occurs in

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