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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, 4-(diethylamino)-2-methyl-

CCN(c1ccc(c(c1)C)C=O)CC Request for Quotation
Chemical Name: Benzaldehyde, 4-(diethylamino)-2-methyl-
CAS Number: 92-14-8
Product Number: AG00IGZ6(AGN-PC-0JL7BX)
Synonyms:
MDL No:
Molecular Formula: C12H17NO
Molecular Weight: 191.2695

Identification/Properties

Properties
BP:
322.5 °C at 760 mmHg
Form:
Solid
Computed Properties
Molecular Weight:
191.274g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
191.131g/mol
Monoisotopic Mass:
191.131g/mol
Topological Polar Surface Area:
20.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
177
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P264-P302+P352-P304+P340-P305+P351+P338-P332+P313-P337+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Diethylamino)-2-methylbenzaldehyde is a versatile compound commonly utilized in chemical synthesis due to its unique properties and reactivity. It serves as a crucial building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. This compound is widely employed as a key intermediate in the synthesis of complex organic molecules, including those with biological activity. Additionally, 4-(Diethylamino)-2-methylbenzaldehyde can participate in a range of reactions, such as condensation, Mannich reactions, and reductive amination, making it a valuable tool for organic chemists seeking to create structurally diverse compounds for various applications in the field of chemistry.