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Key Documents

P16001

Sigma-Aldrich

3-Phenoxypropionic acid

99%

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About This Item

Linear Formula:
C6H5OCH2CH2CO2H
CAS Number:
Molecular Weight:
166.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

powder

bp

235-245 °C (lit.)

mp

98-100 °C (lit.)

SMILES string

OC(=O)CCOc1ccccc1

InChI

1S/C9H10O3/c10-9(11)6-7-12-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)

InChI key

BUSOTUQRURCMCM-UHFFFAOYSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Wayne D Vaccaro et al.
Bioorganic & medicinal chemistry letters, 16(2), 395-399 (2005-10-26)
We report the discovery of novel histamine H(3) receptor antagonists based on 4-[(1H-imidazol-4-yl)methyl]piperidine. The most potent compounds in the series (e.g., 7) result from the attachment of a substituted aniline amide to the main pharmacophore piperidine via a two-methylene linker.
Luc M LeBlanc et al.
Rapid communications in mass spectrometry : RCM, 30(19), 2133-2144 (2016-08-02)
When subjected to collisional activation, gas-phase carboxylate ions typically undergo decarboxylation. However, alternative fragmentation processes dominate when the carboxylate group is located within certain structural motifs. In this work, the fragmentation processes of β-substituted carboxylate ions are characterized to improve

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