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Merck

317519

Sigma-Aldrich

2-乙酰胺基丙烯酸甲酯

98%

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About This Item

线性分子式:
H2C=C(NHCOCH3)CO2CH3
CAS号:
分子量:
143.14
MDL號碼:
分類程式碼代碼:
12162002
PubChem物質ID:
NACRES:
NA.23

化驗

98%

bp

104 °C/8 mmHg (lit.)

mp

50-52 °C (lit.)

SMILES 字串

COC(=O)C(=C)NC(C)=O

InChI

1S/C6H9NO3/c1-4(6(9)10-3)7-5(2)8/h1H2,2-3H3,(H,7,8)

InChI 密鑰

SMWNFFKPVLVOQQ-UHFFFAOYSA-N

一般說明

Conjugated addition of secondary amines, imidazole and pyrazole to methyl 2 methyl 2-acetamidoacrylate in the presence of a catalyst results in the formation of β-Dialkylamino-α-alanine and β-(N-heteroaryl)-α-alanine derivatives. Methyl-2-acetamidoacrylate (M2AA) is an anti-inflammatory agent. The catalytic reaction of methyl 2-acetamidoacrylate with Grignard′s reagents affords α-amino esters. M2AA can form thermosensitive copolymers with methyl acrylate.
Methyl ester of 2-acetamidoacrylate . methyl 2-acetamidoacrylate (Me-2-AA) is a di-unsaturated α-amino acid derivative. methyl-2-acetamidoacrylate exihibits anti -inflammatory properties, it is very effective against lipopolysaccharide (LPS)- induced nitric oxide production by RAW 264.

應用

Methyl 2-acetamidoacrylate can undergo [2+2] cycloaddition (Michael–Dieckmann-type reaction) with ketene diethyl acetal to yield the cyclobutane core. It may be used in rhodium-catalyzed 2-alkenylpyrrole formation.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

235.4 °F - closed cup

閃點(°C)

113 °C - closed cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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William P Hems et al.
Organic & biomolecular chemistry, 3(8), 1547-1550 (2005-04-14)
Rh diphosphine complexes using DuPhos and JosiPhos as chiral ligands have been immobilised by ion exchange into the mesoporous material MCM-41. When used as catalysts for the enantioselective hydrogenation of dimethyl itaconate and methyl-2-acetamidoacrylate, these heterogeneous catalysts give catalytic performance
RhIII?Catalyzed Oxidative Olefination of Vinylic C H Bonds: Efficient and Selective Access to Di?unsaturated ??Amino Acid Derivatives and Other Linear 1, 3?Butadienes.
Besset T, et al.
European Journal of Chemistry, 17(26), 7167-7171 (2011)
Orthogonal synthesis of indolines and isoquinolines via aryne annulation.
Christopher D Gilmore et al.
Journal of the American Chemical Society, 130(5), 1558-1559 (2008-01-16)
FeCl3-catalyzed conjugate addition of secondary amines, imidazole and pyrazole to methyl 2-acetamidoacrylate.
Montserrat P and Pleixats R
Tetrahedron, 51(30), 8355-8362 (1995)
Ethyl pyruvate: a novel anti?inflammatory agent.
Fink MP, et al.
J. Int. Med., 261(4), 349-362 (2007)

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