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10895

2-氯乙酰乙酸乙酯

Name: 2-氯乙酰乙酸乙酯
Brand: ALDRICH

Wacker Chemie AG, ≥96% (GC)

别名:

2-Cl-ACE

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关于此项目

线性分子式:

CH₃COCHClCOOC₂H₅

化学文摘社编号:

609-15-4

分子量:

164.59

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

57646831

EC Number:

210-180-4

Beilstein/REAXYS Number:

774278

MDL number:

MFCD00009141

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属性

assay

≥96% (GC)

manufacturer/tradename

Wacker Chemie AG

refractive index

n20/D 1.441 (lit.)

bp

107 °C/14 mmHg (lit.)

density

1.19 g/mL at 25 °C (lit.)

SMILES string

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

说明

Application

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

Biochem/physiol Actions

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

Other Notes

根据要求提供批量采购价

pictograms

GHS05,GHS07,GHS09

signalword

Danger

hcodes

H302,H314,H335,H400

pcodes

P261 - P273 - P280 - P301 + P312 - P303 + P361 + P353 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

179.6 °F

flash_point_c

82 °C

ppe

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

法规信息

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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)

Analysis of inhibitors of the site-specific recombination reaction mediated by Tn3 resolvase.

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

Fungal aerobic reductive dechlorination of ethyl 2-chloroacetoacetate by Saccharomyces cerevisiae: mechanism of a novel type of microbial dehalogenation.

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).

全球贸易项目编号

货号	GTIN
307610-50G	04061826673706
307610-250G	04061826673690