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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)-

b-Alanine, N,N'-1,2-ethanediylbis[N-(carboxymethyl)-

CCC(=O)O.CCC(=O)O.NCCN(CC(=O)O)CC(=O)O Request for Quotation
Chemical Name: b-Alanine, N,N'-1,2-ethanediylbis[N-(carboxymethyl)-
CAS Number: 32701-19-2
Product Number: AG003QJ2(AGN-PC-0R82AL)
Synonyms:
MDL No:
Molecular Formula: C12H24N2O8
Molecular Weight: 324.3276

Identification/Properties

Properties
MP:
170-175°C
Storage:
2-8℃;Keep in dry area;
Computed Properties
Molecular Weight:
320.298g/mol
XLogP3:
-6.1
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
10
Rotatable Bond Count:
13
Exact Mass:
320.122g/mol
Monoisotopic Mass:
320.122g/mol
Topological Polar Surface Area:
156A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
374
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound $name$, 2,2'-((2-Aminoethyl)azanediyl)diacetic acid with propionic acid (1:2), serves a key role in chemical synthesis as a versatile building block for creating complex organic molecules. This compound can be effectively utilized as a chelating agent for coordinating metal ions in various reactions, enhancing catalytic activity and selectivity. Additionally, the presence of the propionic acid moiety provides a means for functional group manipulation, allowing for further chemical modifications and diversification of the synthesized products. The use of this compound in chemical synthesis enables the efficient construction of novel compounds with tailored properties and functionalities, making it a valuable tool for synthetic chemists seeking to develop innovative materials and bioactive compounds.