产品名称

英文名称：Ethyl (4-Fluorobenzoyl)acetate

同义词

Ethyl 3-(4-Fluorophenyl)-3-Oxopropanoate、1999-00-4、Ethyl 4-fluorobenzoylacetate、Ethyl (4-fluorobenzoyl)acetate、4-Fluorobenzoylacetic acid ethyl ester、BENZENEPROPANOIC ACID, 4-FLUORO-BETA-OXO-, ETHYL ESTER、ETHYL 3-(4-FLUOROPHENYL)-3-OXOPROPIONATE、MFCD03093、4-氟苯甲酰乙酸乙酯

产品性质

CAS编号：1999-00-4

分子式：FC6H4COCH2CO2C2H5

分子量：210.2

MDL号：MFCD03093631

PubChem编号：2758844

别名：4-氟苯甲酰乙酸乙酯

英文别名：Ethyl 3-(4-Fluorophenyl)-3-Oxopropanoate|1999-00-4|Ethyl 4-fluorobenzoylacetate|Ethyl (4-fluorobenzoyl)acetate|4-Fluorobenzoylacetic acid ethyl ester|BENZENEPROPANOIC ACID, 4-FLUORO-BETA-OXO-, ETHYL ESTER|ETHYL 3-(4-FLUOROPHENYL)-3-OXOPROPIONATE|MFCD03093

规格或纯度：>98.0%(GC)

英文名称：Ethyl (4-Fluorobenzoyl)acetate

应用：Reactant used as a precursor in 1.Condensation reactions with diamines via C-C bond cleavage for synthesis of benzimidazoles and perimidines. 2.for possible use as antimalarial treatments 3.Base-promoted domino Michael addition / cyclization / elimination reactions for synthesis of hydroxybenzophenones. 4.Oxidative cross-coupling with indoles via dioxygen activation. 5.Cyclization of keto esters for synthesis of pyrones. 6.Lewis base catalyzed hydrosilylation for synthesis of α-acetoxy β-amino acid derivatives. 7.Conia-ene reactions for synthesis of methylenecyclopentane derivatives.

储存温度：充氩

运输条件：常规运输

产品介绍：Ethyl (4-fluorobenzoyl)acetate on condensation with benzofurazan oxide yields 2-(carboethoxy)-3-(4′-fluoro)phenylquinoxaline1,4-dioxide.Reactant used as a precursor in 1.Condensation reactions with diamines via C-C bond cleavage for synthesis of benzimidazoles and perimidines. 2.for possible use as antimalarial treatments 3.Base-promoted domino Michael addition / cyclization / elimination reactions for synthesis of hydroxybenzophenones. 4.Oxidative cross-coupling with indoles via dioxygen activation. 5.Cyclization of keto esters for synthesis of pyrones. 6.Lewis base catalyzed hydrosilylation for synthesis of α-acetoxy β-amino acid derivatives. 7.Conia-ene reactions for synthesis of methylenecyclopentane derivatives.Ethyl (4-fluorobenzoyl)acetate on condensation with benzofurazan oxide yields 2-(carboethoxy)-3-(4′-fluoro)phenylquinoxaline1,4-dioxide.Reactant used as a precursor in 1.Condensation reactions with diamines via C-C bond cleavage for synthesis of benzimidazoles and perimidines. 2.for possible use as antimalarial treatments 3.Base-promoted domino Michael addition / cyclization / elimination reactions for synthesis of hydroxybenzophenones. 4.Oxidative cross-coupling with indoles via dioxygen activation. 5.Cyclization of keto esters for synthesis of pyrones. 6.Lewis base catalyzed hydrosilylation for synthesis of α-acetoxy β-amino acid derivatives. 7.Conia-ene reactions for synthesis of methylenecyclopentane derivatives.

PubChem SID：488193108

IUPAC Name：ethyl 3-(4-fluorophenyl)-3-oxopropanoate

INCHI：InChI=1S/C11H11FO3/c1-2-15-11(14)7-10(13)8-3-5-9(12)6-4-8/h3-6H,2,7H2,1H3

InChi Key：SJUXLKYJKQBZLM-UHFFFAOYSA-N

Canonical SMILES：CCOC(=O)CC(=O)C1=CC=C(C=C1)F

Isomeric SMILES：CCOC(=O)CC(=O)C1=CC=C(C=C1)F

WGK Germany：3

PubChem CID：2758844

Reaxy-Rn：2212581

密度：1.174

敏感性：对空气敏感

折光率：1.504

沸点：120°C/1mmHg

象形图：

信号词：Warning

危险声明：H315 Causes skin irritationH319 Causes serious eye irritationH335 May cause respiratory irritation

预防措施声明：P261,P305+P351+P338,P280,P302+P352,P321,P405,P501,P264,P271,P304+P340,P403+P233,P362+P364,P264+P265,P337+P317,P332+P317,P319

产品包装