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P16001

3-Phenoxypropionic acid

Name: 3-Phenoxypropionic acid
Brand: ALDRICH

99%

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About This Item

Linear Formula:

C₆H₅OCH₂CH₂CO₂H

CAS Number:

7170-38-9

Molecular Weight:

166.17

NACRES:

NA.22

PubChem Substance ID:

24898220

UNSPSC Code:

12352100

EC Number:

230-518-4

MDL number:

MFCD00002769

Assay:

99%

Form:

powder

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Properties

Quality Level

100

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

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Novel histamine H3 receptor antagonists based on the 4-[(1H-imidazol-4-yl)methyl]piperidine scaffold.

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.

Competing fragmentation processes of β-substituted propanoate ions upon collision-induced dissociation.

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

Global Trade Item Number

SKU	GTIN
P16001-5G	04061831817898