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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)-

Ethanol, 2,2'-[(phenylmethyl)imino]bis-

OCCN(Cc1ccccc1)CCO Request for Quotation
Chemical Name: Ethanol, 2,2'-[(phenylmethyl)imino]bis-
CAS Number: 101-32-6
Product Number: AG0003FI(AGN-PC-0BY33L)
Synonyms:
MDL No:
Molecular Formula: C11H17NO2
Molecular Weight: 195.2582

Identification/Properties

Computed Properties
Molecular Weight:
195.262g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
195.126g/mol
Monoisotopic Mass:
195.126g/mol
Topological Polar Surface Area:
43.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
129
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,2'-(Benzylimino)diethanol, commonly referred to as BINE, is a versatile compound that finds wide applications in chemical synthesis. This compound serves as a chelating ligand in various catalytic reactions, aiding in the formation of stable metal complexes that enhance the efficiency and selectivity of the reaction. In the field of organometallic chemistry, BINE is employed as a ligand in transition metal-catalyzed reactions, such as cross-coupling reactions, C-H activation, and asymmetric catalysis. Its ability to coordinate with various metal ions allows for control over the regioselectivity and stereoselectivity of the reactions. Moreover, BINE's unique structure with a benzyl group and amino alcohol functionality provides an optimal balance of steric and electronic properties, making it a valuable tool in the synthesis of complex organic molecules.