Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

165190

Sigma-Aldrich

O-Acetylsalicyloyl chloride

95%

Sign Into View Organizational & Contract Pricing

Select a Size

5 G
MXP 1,106.00
25 G
MXP 1,749.00

MXP 1,106.00

Check Cart for Availability
Request a Bulk Order
All Photos(1)

Select a Size

Change View
5 G
MXP 1,106.00
25 G
MXP 1,749.00

About This Item

Linear Formula:
2-(CH3CO2)C6H4COCl
CAS Number:
5538-51-2
Molecular Weight:
198.60
Beilstein:
880372
EC Number:
226-899-1
MDL number:
MFCD00000663
UNSPSC Code:
12352100
PubChem Substance ID:
24850129
NACRES:
NA.22

MXP 1,106.00

Check Cart for Availability
Request a Bulk Order

Quality Level

200

Assay

95%

form

solid

refractive index

n20/D 1.536 (lit.)

bp

107-110 °C/0.1 mmHg (lit.)

mp

45-49 °C (lit.)

functional group

acyl chloride
ester

SMILES string

CC(=O)Oc1ccccc1C(Cl)=O

InChI

1S/C9H7ClO3/c1-6(11)13-8-5-3-2-4-7(8)9(10)12/h2-5H,1H3

InChI key

DSGKWFGEUBCEIE-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

  • O-Acetylsalicyloyl chloride was used in the synthesis of enantiomerically pure bidentate heteroorganic ligands built on simple achiral skeletons and containing an aziridine moiety[1].
  • It was used in the general synthesis of acetoxybenzamides[2].
  • It was used in the chemical synthesis of 2,2,6,6-tetramethyl-1-piperidinyloxy(TEMPO)-aspirin conjugate via condensation reaction with 4-hydroxy-TEMPO[3].
  • It was used as reagent in acylation of cyclobutenediones[4].

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

230.0 °F

Flash Point(C)

110 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBP7238V
BCBL7287V
BCBB1151V
BCBB1150V
BCBB1150

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Aziridine ring-containing chiral ligands as highly efficient catalysts in asymmetric synthesis.
Rachwalski M, et al.
Tetrahedron Asymmetry, 24(7), 421-425 (2013)
Wilmarie Flores-Santana et al.
British journal of pharmacology, 165(4b), 1058-1067 (2011-06-11)
Inflammation and reactive oxygen species are associated with the promotion of various cancers. The use of non-steroidal anti-inflammatory drugs (NSAIDs) in cancer prevention treatments has been promising in numerous cancers. We report the evaluation of NSAIDs chemically modified by the
The Journal of Organic Chemistry, 58, 3543-3543 (1993)
Carlos Barea et al.
Bioorganic & medicinal chemistry letters, 21(15), 4498-4502 (2011-07-05)
Continuing with our efforts to identify new active compounds against malaria and leishmaniasis, 14 new 3-amino-1,4-di-N-oxide quinoxaline-2-carbonitrile derivatives were synthesized and evaluated for their in vitro antimalarial and antileishmanial activity against Plasmodium falciparum Colombian FCR-3 strain and Leishmania amazonensis strain

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service