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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)-

(3R,4R)-tert-Butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate

O[C@@H]1CN(C[C@H]1N)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: (3R,4R)-tert-Butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate
CAS Number: 330681-18-0
Product Number: AG00CIRU(AGN-PC-0WA23I)
Synonyms:
MDL No:
Molecular Formula: C9H18N2O3
Molecular Weight: 202.25082

Identification/Properties

Computed Properties
Molecular Weight:
202.254g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
202.132g/mol
Monoisotopic Mass:
202.132g/mol
Topological Polar Surface Area:
75.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
225
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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


The (3R,4R)-tert-Butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate compound plays a crucial role in chemical synthesis as a versatile building block. With its specific stereochemistry and functional groups, this compound serves as a key intermediate in the creation of various complex molecules. In chemical synthesis, the (3R,4R)-tert-Butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate is employed for its ability to participate in a range of reactions, facilitating the formation of new bonds and enabling the construction of structurally diverse compounds. Its unique structural features make it a valuable tool for chemists seeking to access novel chemical entities and explore new avenues in synthetic chemistry.