Home Other Building Blocks 7170-38-9
7170-38-9,MFCD00002769
Catalog No.:AA003JSC

7170-38-9 | 3-Phenoxypropionic acid

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1g
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$7.00   $5.00
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5g
98%
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$11.00   $8.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003JSC
Chemical Name:
3-Phenoxypropionic acid
CAS Number:
7170-38-9
Molecular Formula:
C9H10O3
Molecular Weight:
166.1739
MDL Number:
MFCD00002769
SMILES:
OC(=O)CCOc1ccccc1
Properties
Properties
 
BP:
245°C at 760 mmHg  
Form:
Solid  
MP:
98 - 100 C  
Refractive Index:
1.5184 (estimate)  
Storage:
Room Temperature;Keep in dry area;  

Computed Properties
 
Complexity:
139  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
4  
XLogP3:
1.5  

Upstream Synthesis Route

[1]JournaloftheChemicalSociety,1954,p.4299,4301

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1949,vol.71,p.661

[1]JournaloftheAmericanChemicalSociety,1949,vol.71,p.661

[2]JournaloftheAmericanChemicalSociety,1949,vol.71,p.661

[1]TetrahedronLetters,2018,vol.59,p.869-872

[2]EuropeanJournalofMedicinalChemistry,2010,vol.45,p.25-37

[3]JournaloftheIndianChemicalSociety,1985,vol.62,p.983-989

[4]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1980,vol.<B>19,p.500-503

[5]E-JournalofChemistry,2012,vol.9,p.1251-1256

[6]ChemischeBerichte,1924,vol.57,p.204

[7]JournaloftheAmericanChemicalSociety,1923,vol.45,p.2711

[8]JournaloftheAmericanChemicalSociety,1923,vol.45,p.2711

[9]JournaloftheAmericanChemicalSociety,1923,vol.45,p.2711

[10]ChemischeBerichte,1947,vol.80,p.464,467

[11]ChemischeBerichte,1933,vol.66,p.1168,1175

[12]BulletindelaSocieteChimiquedeFrance,1958,p.325,328

[13]JournaloftheChemicalSociety,1954,p.4299,4301

[14]Farmaco,EdizioneScientifica,1984,vol.39,p.876-887

[15]TetrahedronLetters,2003,vol.44,p.4007-4010

[16]BioorganicandMedicinalChemistryLetters,2013,vol.23,p.310-317

[17]OrganicLetters,2015,vol.17,p.5484-5487

[18]Tetrahedron,2017,vol.73,p.3913-3922

[19]Patent:US4060619,1977,A

[20]MedicinalChemistryResearch,2019,vol.28,p.2184-2199

[1]JournalofOrganicChemistry,1947,vol.12,p.435    JournalofOrganicChemistry,1948,vol.13,p.937

[1]InorganicChemistry,2015,vol.54,p.8685-8692

[2]JournaloftheAmericanChemicalSociety,2002,vol.124,p.6626-6635

[3]ZhurnalObshcheiKhimii,1957,vol.27,p.101,105;engl.Ausg.S.115,119    Chem.Abstr.,1958,p.3728

[4]MonatsheftefurChemie,1967,vol.98,p.1256-1261

[5]JournalofMedicinalChemistry,1994,vol.37,p.1712-1719

[6]ArchivesofPharmacalResearch,2015,vol.38,p.1147-1156

[7]OrganicLetters,2015,vol.17,p.5484-5487

[8]EuropeanJournalofMedicinalChemistry,2019,vol.170,p.141-156

Literature

Title: (R,S)-dichlorprop herbicide in agricultural soil induces proliferation and expression of multiple dioxygenase-encoding genes in the indigenous microbial community.

Journal: Environmental microbiology 20110601

Title: Declining capacity of starving Delftia acidovorans MC1 to degrade phenoxypropionate herbicides correlates with oxidative modification of the initial enzyme.

Journal: Environmental science & technology 20100515

Title: Spectroscopic investigations of the chiral interactions between lipase and the herbicide dichlorprop.

Journal: Chirality 20090301

Title: A phase I and pharmacokinetic study of XK469R (NSC 698215), a quinoxaline phenoxypropionic acid derivative, in patients with refractory acute leukemia.

Journal: Investigational new drugs 20080801

Title: Production of (S)-2-chloropropionate by asymmetric reduction of 2-chloroacrylate with 2-haloacrylate reductase coupled with glucose dehydrogenase.

Journal: Journal of bioscience and bioengineering 20080401

Title: Polymeric sulfated amino acid surfactants: a class of versatile chiral selectors for micellar electrokinetic chromatography (MEKC) and MEKC-MS.

Journal: Analytical chemistry 20070201

Title: The role of autophagy in the death of L1210 leukemia cells initiated by the new antitumor agents, XK469 and SH80.

Journal: Molecular cancer therapeutics 20070101

Title: A supported liquid membrane encapsulating a surfactant-lipase complex for the selective separation of organic acids.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20050204

Title: Thermodynamic approach for studying both the retention and complexation mechanisms with hydroxy-propyl-beta-cyclodextrin of a phenoxy-propionic acid herbicide series.

Journal: Talanta 20041115

Title: In vitro reactivity of carboxylic acid-CoA thioesters with glutathione.

Journal: Chemical research in toxicology 20040101

Title: Use of ionic liquids in a lipase-facilitated supported liquid membrane.

Journal: Biotechnology letters 20030501

Title: Therapeutic androgen receptor ligands.

Journal: Nuclear receptor signaling 20030101

Title: 2-[4-(7-chloro-2-quinoxalinyloxy)phenoxy]-propionic acid (XK469) inhibition of topoisomerase IIbeta is not sufficient for therapeutic response in human Waldenstrom's macroglobulinemia xenograft model.

Journal: Molecular cancer therapeutics 20021201

Title: Chiral discrimination of phenoxypropionic acid herbicide enantiomers on teicoplanin phase: methanol dependence and eluent pH consideration.

Journal: Talanta 20021112

Title: Induction of apoptosis by the new anticancer drug XK469 in human ovarian cancer cell lines.

Journal: Oncogene 20020704

Title: The two enantiospecific dichlorprop/alpha-ketoglutarate-dioxygenases from Delftia acidovorans MC1--protein and sequence data of RdpA and SdpA.

Journal: Microbiological research 20020101

Title: The investigational new drug XK469 induces G(2)-M cell cycle arrest by p53-dependent and -independent pathways.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research 20011101

Title: Physiological and genetic characteristics of two bacterial strains utilizing phenoxypropionate and phenoxyacetate herbicides.

Journal: Microbiological research 20010101

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