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Merck

10895

Sigma-Aldrich

2-氯乙酰乙酸乙酯

produced by Wacker Chemie AG, Burghausen, Germany, Wacker Chemie AG, ≥96% (GC)

别名:

2-Cl-ACE

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About This Item

线性分子式:
CH3COCHClCOOC2H5
CAS号:
分子量:
164.59
Beilstein:
774278
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

等级

produced by Wacker Chemie AG, Burghausen, Germany

方案

≥96% (GC)

制造商/商品名称

Wacker Chemie AG

折射率

n20/D 1.441 (lit.)

沸点

107 °C/14 mmHg (lit.)

密度

1.19 g/mL at 25 °C (lit.)

SMILES字符串

CCOC(=O)C(Cl)C(C)=O

InChI

1S/C6H9ClO3/c1-3-10-6(9)5(7)4(2)8/h5H,3H2,1-2H3

InChI key

RDULEYWUGKOCMR-UHFFFAOYSA-N

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应用

Ethyl 2-chloroacetoacetate was used to study reductive dechlorination of β-keto ester ethyl 2-chloroacetoacetate by Saccharomyces cerevisiae.

生化/生理作用

Ethyl 2-chloroacetoacetate reacts with thiosemicarbazones to form heterocyclic substituted thiophene derivatives having non-steroidal anti-inflammatory activity.

其他说明

根据要求提供批量采购价

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

179.6 °F

闪点(°C)

82 °C

个人防护装备

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Synthesis and antiinflammatory activity of novel 2, 5-disubstituted thiophene derivatives.
Badr SMI.
Turkish Journal of Chemistry, 35(1), 131-143 (2011)
P M Flanagan et al.
Journal of molecular biology, 206(2), 295-304 (1989-03-20)
The Tn3-encoded resolvase protein promotes a site-specific recombination reaction between two directly repeated copies of the recombination site res. Several inhibitors that block this event in vitro have been isolated. In this study four of these inhibitors were tested on
Gerhard Jörg et al.
Chembiochem : a European journal of chemical biology, 5(1), 87-92 (2003-12-26)
Saccharomyces cerevisiae reduces the beta-keto ester ethyl 2-chloroacetoacetate to the respective chiral cis- and trans-beta-hydroxy esters. In the course of chiral reduction, competing dehalogenation of the xenobiotic substrate to ethyl acetoacetate occurs, in a reaction mediated by cytosolic glutathione (GSH).

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