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474533

Sigma-Aldrich

(R)-(+)-2-(4-Hydroxyphenoxy)propionic acid

98%

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25 G
₪217.00

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25 G
₪217.00

About This Item

Linear Formula:
CH3CH(OC6H4OH)CO2H
CAS Number:
94050-90-5
Molecular Weight:
182.17
EC Number:
407-960-3
MDL number:
MFCD00274088
UNSPSC Code:
12352112
PubChem Substance ID:
24871017
NACRES:
NA.22

₪217.00

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Quality Level

100

Assay

98%

form

solid

optical activity

[α]20/D +58°, c = 1 in methanol

mp

145-148 °C (lit.)

functional group

carboxylic acid

SMILES string

C[C@@H](Oc1ccc(O)cc1)C(O)=O

InChI

1S/C9H10O4/c1-6(9(11)12)13-8-4-2-7(10)3-5-8/h2-6,10H,1H3,(H,11,12)/t6-/m1/s1

InChI key

AQIHDXGKQHFBNW-ZCFIWIBFSA-N

Related Categories

Application

(R)-2-(4-Hydroxyphenoxy)propionic acid can be used as a ligand to prepare:
  • Triorganotin(IV) complexes of biological importance.[1]
  • Co(II) based chiral coordination polymers having catalytic activity towards aldol reaction.[2]

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H318

Precautionary Statements

P280 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR8506
MKCK8745
MKBT5421V
MKBG9168V
04915LD

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Syntheses, characterizations, crystal structures, and in vitro antitumor activities of chiral triorganotin (IV) complexes containing (S)-(+)-2-(4-isobutyl-phenyl) propionic and (R)-(+)-2-(4-hydroxyphenoxy) propionic acid ligands
Shi Y, et al.
Journal of Coordination Chemistry, 65(23), 4125-4136 (2012)
Rosalía López-Ruiz et al.
Ecotoxicology and environmental safety, 157, 285-291 (2018-04-09)
A degradation study of quizalofop-p and its commercial products (quizalofop-p-ethyl, quizalofop-p-tefuryl and propaquizafop) in water samples has been performed using ultra high-performance liquid chromatography coupled to Orbitrap mass spectrometry (UHPLC-Orbitrap-MS). CHHQ (dihydroxychloroquinoxalin), CHQ (6-chloroquinoxalin-2-ol) and PPA ((R)-2-(4-hydroxyphenoxy)propionicacid) were the main
Syntheses, structures and catalytic properties of chiral Co (II) coordination polymers based on (R)-4-(4-(1-carboxyethoxy) phenoxy) benzoic acid
Xu X, et al.
Polyhedron, 112(23), 61-66 (2016)

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