1. Home
  2. Benzaldehyde, 2-chloro-3-(trifluoromethyl)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Benzaldehyde, 2-chloro-3-(trifluoromethyl)-

O=Cc1cccc(c1Cl)C(F)(F)F Request for Quotation
Chemical Name: Benzaldehyde, 2-chloro-3-(trifluoromethyl)-
CAS Number: 93118-03-7
Product Number: AG00337B(AGN-PC-0KK7ZL)
Synonyms:
MDL No: MFCD00792414
Molecular Formula: C8H4ClF3O
Molecular Weight: 208.5650

Identification/Properties

Properties
MP:
37-43 °C(lit.)
BP:
216.6 °C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Air Sensitive
Computed Properties
Molecular Weight:
208.564g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
207.99g/mol
Monoisotopic Mass:
207.99g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
192
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Chloro-3-(trifluoromethyl)benzaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis processes. This chemical plays a crucial role as a building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. It serves as a key intermediate in the preparation of complex organic molecules due to its unique structural properties.In organic synthesis, 2-Chloro-3-(trifluoromethyl)benzaldehyde acts as a valuable precursor for the introduction of functional groups such as chloro, trifluoromethyl, and benzaldehyde moieties into target molecules. Its reactivity allows for selective transformations, making it a valuable tool for chemists in designing and creating intricate chemical structures. This compound is particularly useful in the development of new drugs, herbicides, and other biologically active compounds due to its ability to introduce specific functionalities with high precision.Furthermore, 2-Chloro-3-(trifluoromethyl)benzaldehyde's versatility extends to its application in material science, where it serves as a starting material for the synthesis of novel polymers, dyes, and functional materials. Its unique chemical properties make it a favored choice for researchers seeking to tailor molecular structures for specific applications, demonstrating its importance in advancing various fields of chemistry.Overall, the strategic use of 2-Chloro-3-(trifluoromethyl)benzaldehyde in chemical synthesis highlights its significance as a foundational component in creating diverse chemical entities with tailored properties and potential applications across multiple industries.