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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)-

4-[(4-amino-3-ethyl-phenyl)methyl]-2-ethyl-aniline

CCc1cc(ccc1N)Cc1ccc(c(c1)CC)N Request for Quotation
Chemical Name: 4-[(4-amino-3-ethyl-phenyl)methyl]-2-ethyl-aniline
CAS Number: 19900-65-3
Product Number: AG002BVG(AGN-PC-0JLXC4)
Synonyms:
MDL No:
Molecular Formula: C17H22N2
Molecular Weight: 254.3700

Identification/Properties

Properties
MP:
45.5-46.5℃(Solv: hexane (110-54-3); benzene (71-43-2)(1:1))
BP:
426°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
1.5794 (estimate)
Computed Properties
Molecular Weight:
254.377g/mol
XLogP3:
4.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
254.178g/mol
Monoisotopic Mass:
254.178g/mol
Topological Polar Surface Area:
52A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
240
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,4'-Methylenebis(2-ethylaniline) is a crucial compound commonly utilized in chemical synthesis processes. It serves as a primary building block in the production of various polymers, resins, and dyes. Due to its unique molecular structure, this compound exhibits excellent reactivity and functionality, making it a versatile ingredient in the creation of advanced materials.In organic synthesis, 4,4'-Methylenebis(2-ethylaniline) plays a key role as a crosslinking agent in the formulation of polyurethane and epoxy resins. Its presence facilitates the formation of strong, durable bonds, enhancing the mechanical and thermal properties of the final polymer products. Moreover, this compound is instrumental in the synthesis of specialty chemicals, such as antioxidants and corrosion inhibitors, which find applications in coatings, adhesives, and industrial processes.Furthermore, 4,4'-Methylenebis(2-ethylaniline) is employed in the manufacturing of dyes and pigments due to its ability to impart vibrant color and excellent lightfastness to various materials. By incorporating this compound into the dye synthesis process, chemists can achieve a wide range of shades and hues with superior color retention properties.Overall, the utilization of 4,4'-Methylenebis(2-ethylaniline) in chemical synthesis enhances the quality, performance, and versatility of a diverse array of products across industries, showcasing its significance as a valuable component in modern material science.