Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

516333

Sigma-Aldrich

4-Acetylbenzaldehyde

97%

Synonym(s):

4-Formylacetophenone

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3COC6H4CHO
CAS Number:
3457-45-2
Molecular Weight:
148.16
MDL number:
MFCD02093689
UNSPSC Code:
12352100
PubChem Substance ID:
24873881
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

33-36 °C (lit.)

SMILES string

[H]C(=O)c1ccc(cc1)C(C)=O

InChI

1S/C9H8O2/c1-7(11)9-4-2-8(6-10)3-5-9/h2-6H,1H3

InChI key

KTFKRVMXIVSARW-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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SHBJ6253
SHBF3988V
SHBB8733V
55696LM
25596LK

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

Bis [(tetraphenylporphyrinato) zinc]-calix [4] pyrrole. Synthesis and receptor properties.
Mamardashvili NZ, et al.
Russ. J. Org. Chem., 50(4), 559-566 (2014)
Selective reduction of less reactive carbonyl groups in the presence of diborane and sodium bisulfite on silica gel.
Chihara T, et al.
Canadian Journal of Chemistry, 68(5), 720-724 (1990)
Application of the combination of sodium bisulfite as a protective reagent and solid supports in the selective reduction of 4-acetylbenzaldehyde with diborane.
Chihara T, et al.
Chemistry Letters (Jpn), 11, 1657-1660 (1981)
NaBH4/NaNO3/H2O: A Convenient System for Selective Reduction of Aldehydes VS. Ketones to their Corresponding Alcohols.
Ghaderi S and Setamdideh D.
Orient. J. Chem., 30(4), 1913-1917 (2014)
Low-Pressure Hydrogenation of Arenecarboxylic Acids to Aryl Aldehydes.
Goo?en LJ, et al.
Advanced Synthesis & Catalysis, 352(13), 2166-2170 (2010)

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