1. Home
  2. 5-[3-(trifluoromethyl)phenyl]thiophene-2-carbaldehyde

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)-

5-[3-(trifluoromethyl)phenyl]thiophene-2-carbaldehyde

O=Cc1ccc(s1)c1cccc(c1)C(F)(F)F Request for Quotation
Chemical Name: 5-[3-(trifluoromethyl)phenyl]thiophene-2-carbaldehyde
CAS Number: 886508-92-5
Product Number: AG003MB6(AGN-PC-0LF95H)
Synonyms:
MDL No: MFCD06410192
Molecular Formula: C12H7F3OS
Molecular Weight: 256.2436

Identification/Properties

Properties
Storage:
2-8℃;Inert atmosphere;
Computed Properties
Molecular Weight:
256.242g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
256.017g/mol
Monoisotopic Mass:
256.017g/mol
Topological Polar Surface Area:
45.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
279
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

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


5-(3-(Trifluoromethyl)phenyl)thiophene-2-carbaldehyde is a versatile compound widely used in chemical synthesis. This compound is often employed as a key building block in the preparation of various pharmaceuticals and agrochemicals due to its unique chemical properties. Its functional groups allow for selective reactions, enabling the formation of complex molecular structures with high efficiency. In organic synthesis, this compound serves as a valuable intermediate in the production of diverse organic compounds, contributing to the development of new materials and bioactive molecules. Additionally, 5-(3-(Trifluoromethyl)phenyl)thiophene-2-carbaldehyde plays a crucial role in the synthesis of advanced materials and fine chemicals, showcasing its significance in the field of chemistry.