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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)-

[1,1'-Biphenyl]-3-carboxaldehyde, 2',6'-dimethyl-

O=Cc1cccc(c1)c1c(C)cccc1C Request for Quotation
Chemical Name: [1,1'-Biphenyl]-3-carboxaldehyde, 2',6'-dimethyl-
CAS Number: 691905-26-7
Product Number: AG003G9H(AGN-PC-03YL4K)
Synonyms:
MDL No:
Molecular Formula: C15H14O
Molecular Weight: 210.2711

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
210.276g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
210.104g/mol
Monoisotopic Mass:
210.104g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
226
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2',6'-Dimethylbiphenyl-3-carbaldehyde is a versatile compound widely used in chemical synthesis. Its unique structure allows it to be utilized in various reactions for the preparation of complex organic molecules. In particular, this compound serves as a key building block in the synthesis of biologically active compounds, pharmaceuticals, and advanced materials.Due to its aromatic nature and functional group positioning, 2',6'-Dimethylbiphenyl-3-carbaldehyde can participate in numerous reactions such as Friedel-Crafts acylation, Grignard reactions, and Heck couplings. These reactions enable the introduction of important functional groups and structural modifications, making it a valuable tool for organic chemists.Furthermore, the presence of the aldehyde group in 2',6'-Dimethylbiphenyl-3-carbaldehyde allows for selective and specific transformations, leading to the formation of intricate chemical structures with high efficiency. This compound has found applications in the synthesis of natural products, dyes, and heterocyclic compounds, demonstrating its significance in modern organic chemistry.In summary, 2',6'-Dimethylbiphenyl-3-carbaldehyde plays a crucial role in chemical synthesis by enabling the construction of complex molecules with tailored properties and functionalities. Its versatility and reactivity make it an indispensable component in the toolkit of synthetic chemists striving to develop novel compounds for various applications.