1. Home
  2. 2,6-dichloro-4-fluorobenzaldehyde

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2,6-dichloro-4-fluorobenzaldehyde

O=Cc1c(Cl)cc(cc1Cl)F Request for Quotation
Chemical Name: 2,6-dichloro-4-fluorobenzaldehyde
CAS Number: 1182709-86-9
Product Number: AG003G2V(AGN-PC-09TBSR)
Synonyms:
MDL No:
Molecular Formula: C7H3Cl2FO
Molecular Weight: 193.0025

Identification/Properties

Properties
BP:
235.5±35.0°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
192.998g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
191.954g/mol
Monoisotopic Mass:
191.954g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
141
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

PNMR/2_6-DICHLORO-4-FLUOROBENZALDEHYDE_1182709-86-9_hnmr.pdf

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2,6-Dichloro-4-fluorobenzaldehyde is a versatile compound widely used in chemical synthesis as a key intermediate. Known for its unique chemical properties, this compound plays a crucial role in various organic reactions, including the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its reactivity and functional groups make it a valuable building block for creating complex molecular structures with specific desired properties. In organic synthesis, 2,6-Dichloro-4-fluorobenzaldehyde acts as a key starting material for the preparation of diverse compounds, making it an essential component in the development of new molecules for a range of industrial applications.