Home Halogens 3-(2,4-dichlorophenoxy)propanoic acid

3-(2,4-dichlorophenoxy)propanoic acid

CAS No.:
3284-80-8
Catalog Number:
AG019V7F
Molecular Formula:
C9H8Cl2O3
Molecular Weight:
235.0640
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Product Description
Catalog Number:
AG019V7F
Chemical Name:
3-(2,4-dichlorophenoxy)propanoic acid
CAS Number:
3284-80-8
Molecular Formula:
C9H8Cl2O3
Molecular Weight:
235.0640
MDL Number:
MFCD00152417
IUPAC Name:
3-(2,4-dichlorophenoxy)propanoic acid
InChI:
InChI=1S/C9H8Cl2O3/c10-6-1-2-8(7(11)5-6)14-4-3-9(12)13/h1-2,5H,3-4H2,(H,12,13)
InChI Key:
XHUAIKXCACQSGV-UHFFFAOYSA-N
SMILES:
OC(=O)CCOc1ccc(cc1Cl)Cl
Properties
Complexity:
199  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
233.985g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
235.06g/mol
Monoisotopic Mass:
233.985g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
46.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.2  
Literature
Title Journal
Acyl substrate preferences of an IAA-amido synthetase account for variations in grape (Vitis vinifera L.) berry ripening caused by different auxinic compounds indicating the importance of auxin conjugation in plant development. Journal of experimental botany 20110801
Uptake kinetics of 2,4-dichlorophenoxyacetate by Delftia acidovorans MC1 and derivative strains: complex characteristics in response to pH and growth substrate. Bioscience, biotechnology, and biochemistry 20060701
Rapid chromatographic methods for the identification and determination of chlorophenoxy herbicides. Medicinski arhiv 20050101
Regulation of catabolic enzymes during long-term exposure of Delftia acidovorans MC1 to chlorophenoxy herbicides. Microbiology (Reading, England) 20040401
Delftia acidovorans MC1 resists high herbicide concentrations--a study of nutristat growth on (RS)-2-(2,4-Dichlorophenoxy)propionate and 2,4-dichlorophenoxyacetate. Bioscience, biotechnology, and biochemistry 20040301
Synergy of combining sonolysis and photocatalysis in the degradation and mineralization of chlorinated aromatic compounds. Environmental science & technology 20030501
Intercalibration of chromatographic methods for auxino phytodrugs in Solanaceae. Journal of chromatography. A 20030418
Assimilatory detoxification of herbicides by Delftia acidovorans MC1: induction of two chlorocatechol 1,2-dioxygenases as a response to chemostress. Microbiology (Reading, England) 20020901
Properties