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About This Item
Linear Formula:
Cl2C6H3CHO
CAS Number:
Molecular Weight:
175.01
Beilstein:
2040553
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
mp
63.5-65.5 °C (lit.)
SMILES string
[H]C(=O)c1cc(Cl)cc(Cl)c1
InChI
1S/C7H4Cl2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H
InChI key
CASRSOJWLARCRX-UHFFFAOYSA-N
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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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1A
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Certificates of Analysis (COA)
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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)
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