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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)-

Ampicillin Amino-benzeneacetaldehyde

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Chemical Name: Ampicillin Amino-benzeneacetaldehyde
CAS Number: 10001-82-8
Product Number: AG01DZAC(AGN-PC-0WP1A9)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
482.555g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
7
Exact Mass:
482.162g/mol
Monoisotopic Mass:
482.162g/mol
Topological Polar Surface Area:
167A^2
Heavy Atom Count:
34
Formal Charge:
0
Complexity:
824
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
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


Ampicillin antibacterial agent is a semi-synthetic penicillin derivative that contains an amino group and a benzene ring in its chemical structure. When Ampicillin is broken down in the body, one of the metabolites produced is amino-benzeneacetaldehyde.In chemical synthesis, amino-benzeneacetaldehyde can serve as a valuable building block for the creation of various compounds. This versatile compound can participate in reactions like condensation, reduction, and oxidation to form new organic molecules. Its amino group can be further functionalized to introduce different chemical groups, expanding the potential applications in the synthesis of pharmaceuticals, agrochemicals, and materials.The presence of the benzene ring provides aromatic properties, making amino-benzeneacetaldehyde useful in the development of aromatic compounds and optimizing electronic and steric properties of the final products. Additionally, the aldehyde functional group offers opportunities for selective transformations to introduce new functionalities, enhancing the versatility of amino-benzeneacetaldehyde in chemical transformations.Overall, amino-benzeneacetaldehyde plays a crucial role in organic synthesis, offering chemists a key intermediate to access a wide range of structurally diverse compounds with potential applications in various industries.