Skip to Content
Merck
All Photos(1)

Documents

265179

Sigma-Aldrich

2,4-Difluorobenzaldehyde

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
F2C6H3CHO
CAS Number:
Molecular Weight:
142.10
Beilstein:
2243422
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

liquid

refractive index

n20/D 1.498 (lit.)

bp

65-66 °C/17 mmHg (lit.)

mp

2-3 °C (lit.)

density

1.299 g/mL at 25 °C (lit.)

SMILES string

[H]C(=O)c1ccc(F)cc1F

InChI

1S/C7H4F2O/c8-6-2-1-5(4-10)7(9)3-6/h1-4H

InChI key

WCGPCBACLBHDCI-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

The emission and absorption spectra of 2,4-difluorobenzaldehyde were studied.

Application

2,4-Difluorobenzaldehyde was used in the synthesis of 3-benzylidene 20,29-dihydrobetulinic acid derivatives.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

131.0 °F - closed cup

Flash Point(C)

55 °C - closed cup

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’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 6

1 of 6

Spectroscopy and dynamics of the excited singlet and triplet states of 2, 3-, 2, 4-and 2, 5-difluorobenzaldehyde vapors.
Itoh, T.
Journal of Molecular Spectroscopy, 257(2), 170-176 (2009)
Rama Mukherjee et al.
Bioorganic & medicinal chemistry letters, 14(12), 3169-3172 (2004-05-20)
New 3-O-acyl, 3-benzylidene, 3-hydrazone, 3-hydrazine, 17-carboxyacryloyl ester derivatives of betulinic acid (2-6, 8-11, 13, 17, 18, 21, and 22) were synthesized and evaluated in vitro for anti-angiogenic activity on endothelial cell cytotoxicity, specificity, and tube-formation ability. All derivatives reported here

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