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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-(2-thienyl)-

O=Cc1ccccc1c1cccs1 Request for Quotation
Chemical Name: Benzaldehyde, 2-(2-thienyl)-
CAS Number: 99902-07-5
Product Number: AG003VM8(AGN-PC-0KL7MA)
Synonyms:
MDL No:
Molecular Formula: C11H8OS
Molecular Weight: 188.2456

Identification/Properties

Properties
BP:
331°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
188.244g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
188.03g/mol
Monoisotopic Mass:
188.03g/mol
Topological Polar Surface Area:
45.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
181
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Thiophen-2-yl)benzaldehyde, also known as Thiophene-2-carbaldehyde, is a versatile compound widely used in chemical synthesis applications. With its unique structure combining a thiophene ring with a benzaldehyde group, this compound offers several valuable properties that make it an essential building block in organic chemistry.In chemical synthesis, 2-(Thiophen-2-yl)benzaldehyde serves as a key intermediate in the production of various organic compounds. Its reactive aldehyde group allows it to participate in a wide range of reactions, including condensation, oxidation, and reduction processes. This versatility makes it valuable for creating complex molecules with specific functionalities.One common application of 2-(Thiophen-2-yl)benzaldehyde is in the synthesis of pharmaceuticals and agrochemicals. Its unique molecular structure can be modified through various chemical reactions to introduce specific functional groups or enhance biological activity. This makes it an important precursor in the development of new drugs and crop protection agents.Additionally, 2-(Thiophen-2-yl)benzaldehyde is used in material science for synthesizing organic electronics, polymers, and dyes. Its aromatic ring system and electron-rich sulfur atom provide favorable properties for constructing advanced materials with tailored properties such as conductivity, optical activity, and solubility.Overall, the versatility of 2-(Thiophen-2-yl)benzaldehyde makes it a valuable tool in chemical synthesis, enabling the creation of diverse organic molecules with applications in pharmaceuticals, agrochemicals, and materials science.