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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)-

1H-Tetrazole-5-acetic acid, a-amino-

OC(=O)C(c1n[nH]nn1)N Request for Quotation
Chemical Name: 1H-Tetrazole-5-acetic acid, a-amino-
CAS Number: 138199-51-6
Product Number: AG00189J(AGN-PC-0PMC1J)
Synonyms:
MDL No: MFCD00233633
Molecular Formula: C3H5N5O2
Molecular Weight: 143.1041

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
143.106g/mol
XLogP3:
-4.1
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
143.044g/mol
Monoisotopic Mass:
143.044g/mol
Topological Polar Surface Area:
118A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
139
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-Amino-2-(2H-tetrazol-5-yl)acetic acid, commonly referred to as $name$, is a versatile compound that finds wide application in chemical synthesis. This compound serves as a valuable building block in the production of various complex molecules due to its unique structural properties and reactivity. In organic synthesis, $name$ is frequently employed as a key intermediate for the preparation of pharmaceuticals, agrochemicals, and materials with diverse functionalities. Its amino and tetrazole groups provide opportunities for selective derivatization, allowing chemists to introduce specific functional groups or stereochemical motifs into target molecules. Additionally, the presence of the tetrazole ring in 2-Amino-2-(2H-tetrazol-5-yl)acetic acid imparts enhanced stability and bioactivity to the final products, making it a preferred choice in drug discovery and development efforts. This compound's utility extends beyond pharmaceuticals to include the synthesis of advanced materials, dyes, and complex organic compounds, showcasing its significance in modern chemical research and industrial applications.