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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)-

1-Pyrrolidineaceticacid, 3-hydroxy-

OC1CCN(C1)CC(=O)O Request for Quotation
Chemical Name: 1-Pyrrolidineaceticacid, 3-hydroxy-
CAS Number: 258530-57-3
Product Number: AG00BHOY(AGN-PC-02KIHI)
Synonyms:
MDL No:
Molecular Formula: C6H11NO3
Molecular Weight: 145.1564

Identification/Properties

Computed Properties
Molecular Weight:
145.158g/mol
XLogP3:
-2.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
145.074g/mol
Monoisotopic Mass:
145.074g/mol
Topological Polar Surface Area:
60.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
137
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H312-H332
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(3-Hydroxypyrrolidin-1-yl)acetic acid, also known as hydroxyproline, is a valuable compound widely utilized in chemical synthesis, particularly in the field of organic chemistry. This compound plays a crucial role as a building block in the synthesis of peptides and proteins due to its unique structure and functional groups. Hydroxyproline is commonly used in the production of collagen and as a chiral source in various asymmetric synthesis reactions. Its presence in peptide sequences imparts stability and rigidity, making it essential in the study and design of bioactive compounds. In the pharmaceutical industry, (3-Hydroxypyrrolidin-1-yl)acetic acid finds applications in the development of new drugs and therapeutic agents with improved biological activity and target specificity. Additionally, it serves as a key intermediate in the preparation of enzyme inhibitors, peptide mimetics, and other bioactive molecules with potential pharmaceutical applications. The versatility and significance of hydroxyproline in chemical synthesis highlight its importance as a valuable tool for researchers and chemists working in the design and production of novel compounds with diverse applications.