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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)-

2-(2-aminoethoxy)acetic acid hydrochloride

NCCOCC(=O)O.Cl Request for Quotation
Chemical Name: 2-(2-aminoethoxy)acetic acid hydrochloride
CAS Number: 81142-16-7
Product Number: AG01A6Q6(AG01A6Q6)
Synonyms:
MDL No:
Molecular Formula: C4H10ClNO3
Molecular Weight: 155.5801

Identification/Properties

Computed Properties
Molecular Weight:
155.578g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
155.035g/mol
Monoisotopic Mass:
155.035g/mol
Topological Polar Surface Area:
72.6A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
73.7
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(2-Aminoethoxy)acetic acid hydrochloride, also known as glycine ethyl ester hydrochloride, is a versatile compound used in various chemical synthesis processes. This compound serves as a key building block in the creation of pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structure and reactivity. In chemical synthesis, 2-(2-Aminoethoxy)acetic acid hydrochloride acts as a crucial intermediate in the formation of complex organic molecules through its ability to undergo various reactions such as esterification, amidation, and alkylation. Its versatile nature allows for the modification of its functional groups, enabling chemists to tailor its properties for specific applications. Additionally, this compound plays a significant role in the synthesis of amino acid derivatives, peptide synthesis, and drug development, making it an essential component in the arsenal of synthetic chemists.