609-15-4 | Ethyl 2-chloroacetoacetate

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$8.00	$5.00
25g	95%	in stock	$21.00	$15.00
100g	95%	in stock	$35.00	$24.00

Description

• Catalog Number: AB46050
• Chemical Name: Ethyl 2-chloroacetoacetate
• CAS Number: 609-15-4
• Molecular Formula: C6H9ClO3
• Molecular Weight: 164.5869
• MDL Number: MFCD00009141
• SMILES: CCOC(=O)C(C(=O)C)Cl
• NSC Number: 78426

Computed Properties

• Complexity: 144
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.1

Literature

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  International journal of molecular sciences 20120101

• K2CO3-promoted domino reactions: construction of functionalized 2,3-dihydrobenzofurans and clofibrate analogues.

  The Journal of organic chemistry 20110902

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  Acta crystallographica. Section E, Structure reports online 20110801

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  Acta crystallographica. Section E, Structure reports online 20110801

• 1-Chloro-1-[(4-nitro-phen-yl)hydrazinyl-idene]propan-2-one.

  Acta crystallographica. Section E, Structure reports online 20110801

• 1-Chloro-1-[(4-methyl-phen-yl)hydrazinyl-idene]propan-2-one.

  Acta crystallographica. Section E, Structure reports online 20110801

• Ethyl (Z)-2-chloro-2-(2-phenyl-hydrazin-1-yl-idene)acetate.

  Acta crystallographica. Section E, Structure reports online 20100901

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  Acta crystallographica. Section E, Structure reports online 20100901

• Syntheses of aromatic substituted hydrazino-thiazole derivatives to clarify structural characterization and antioxidant activity between 3-arylsydnonyl and aryl substituted hydrazino-thiazoles.

  Chemical & pharmaceutical bulletin 20070801

• Stereoselective, biocatalytic reductions of alpha-chloro-beta-keto esters.

  The Journal of organic chemistry 20050107

• Syntheses and evaluation of antioxidant activity of sydnonyl substituted thiazolidinone and thiazoline derivatives.

  Bioorganic & medicinal chemistry 20040901

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

  Chembiochem : a European journal of chemical biology 20040103

• Synthesis and in vitro antibacterial evaluation of novel imidazo[2',1':5,1]-1,2,4-triazolo[4,3-c]-quinazoline derivatives of 5-thioxo-1, 2, 4-triazole, 4-oxothiazolidine, and their open-chain counterparts.

  Archiv der Pharmazie 20031201