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253839

3-Acetylbenzoic acid

Name: 3-Acetylbenzoic acid
Brand: ALDRICH

98%

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About This Item

Linear Formula:

CH₃COC₆H₄CO₂H

CAS Number:

586-42-5

Molecular Weight:

164.16

NACRES:

NA.22

PubChem Substance ID:

24855333

UNSPSC Code:

12352100

MDL number:

MFCD00045847

Assay:

98%

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Properties

Quality Level

100

assay

98%

mp

169-171 °C (lit.)

functional group

carboxylic acid, ketone

SMILES string

CC(=O)c1cccc(c1)C(O)=O

InChI

1S/C9H8O3/c1-6(10)7-3-2-4-8(5-7)9(11)12/h2-5H,1H3,(H,11,12)

InChI key

CHZPJUSFUDUEMZ-UHFFFAOYSA-N

Description

Application

3-Acetylbenzoic acid has been used in preparation of 3-(2-hydroxyethyl)benzyl alcohol and methyl 3-acetylbenzoate.

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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Synthesis, SAR study and biological evaluation of novel pyrazolo[1,5-a]pyrimidin-7-yl phenyl amides as anti-proliferative agents.

Yanong D Wang et al.

Bioorganic & medicinal chemistry, 17(5), 2091-2100 (2009-02-10)

Checkpoint deficiency of malignant cells can be exploited in cancer drug discovery. Compounds that selectively kill checkpoint-deficient cells versus checkpoint-proficient cells can be utilized to preferentially target tumor cells, while sparing normal cells. The protein p21(Wafl/Cipl/Sdi1) (hereafter referred to as

Evaluation of the NO-releasing properties of NO-donor linkers.

Vincenzo Calderone et al.

The Journal of pharmacy and pharmacology, 60(2), 189-195 (2008-02-02)

This work describes the synthesis of some benzoic (1-4) and alcoholic (5-7) nitrooxy derivatives, which are nitric oxide (NO) donors in themselves, and can also be seen as useful linkers that can be used in multi-target drugs capable of releasing

Global Trade Item Number

SKU	GTIN
253839-1G	04061825584072
253839-5G	04061831819342