139408
3,5-Dichlorobenzaldehyde
97%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
Cl2C6H3CHO
CAS Number:
Molecular Weight:
175.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
233-499-0
Beilstein/REAXYS Number:
2040553
MDL number:
Assay:
97%
InChI key
CASRSOJWLARCRX-UHFFFAOYSA-N
InChI
1S/C7H4Cl2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H
SMILES string
[H]C(=O)c1cc(Cl)cc(Cl)c1
assay
97%
mp
63.5-65.5 °C (lit.)
functional group
aldehyde, chloro
Application
3,5-Dichlorobenzaldehyde was used as starting reagent during synthesis of β-aryl-β-amino acid enantiomers. It was used in the synthesis of dichlorophenylpyruvic acid.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1A
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
An efficient new enzymatic method for the preparation of ?-aryl-?-amino acid enantiomers.
Tasnadi G, et al.
Tetrahedron Asymmetry, 19(17), 2072-2077 (2008)
The effect of 4-hydroxyl substituent on the singlet chemiexcitation yield in base-catalyzed air oxidation of 3, 5-dichlorophenylpyruvic acids.
Kamiya I, et al.
Bulletin of the Chemical Society of Japan, 57(7), 1740-1744 (1984)
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