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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)-

Butanoic acid, 2,2'-(1,2-ethanediyldiimino)bis-

CCC(C(=O)O)NCCNC(C(=O)O)CC Request for Quotation
Chemical Name: Butanoic acid, 2,2'-(1,2-ethanediyldiimino)bis-
CAS Number: 498-17-9
Product Number: AG0032W3(AGN-PC-0JPOJH)
Synonyms:
MDL No:
Molecular Formula: C10H20N2O4
Molecular Weight: 232.2768

Identification/Properties

Properties
MP:
>271°C (dec.)
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
232.28g/mol
XLogP3:
-4.1
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
9
Exact Mass:
232.142g/mol
Monoisotopic Mass:
232.142g/mol
Topological Polar Surface Area:
98.7A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
209
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,2′-(Ethylenediimino)dibutyric acid, also known as EDDA, is a versatile compound widely utilized in chemical synthesis. This compound serves as a crucial ligand in coordination chemistry, forming coordination complexes with various metal ions. In organic synthesis, EDDA acts as a chelating agent, enhancing the efficiency of certain reactions by chelating metal ions and facilitating bond formation. Additionally, EDDA is utilized in catalysis as a stabilizer for metal catalysts, improving the overall yield and selectivity of reactions. Furthermore, EDDA is employed in the preparation of metal-organic frameworks (MOFs), where its chelating properties aid in the construction of well-defined structures with diverse applications in materials science and catalysis.