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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)-

tert-butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate

OC1CN(CC1N)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate
CAS Number: 190141-99-2
Product Number: AG002ED9(AGN-PC-004U4Y)
Synonyms:
MDL No:
Molecular Formula: C9H18N2O3
Molecular Weight: 202.2508

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:
0
Undefined Atom Stereocenter Count:
2
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 tert-Butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate compound is a versatile chemical reagent commonly used in chemical synthesis processes. This compound serves as an important building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and properties make it particularly valuable in organic chemistry reactions. By incorporating tert-Butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate into synthesis pathways, chemists can achieve regioselective and stereoselective transformations, enabling the efficient production of complex molecules with high purity and yield. Furthermore, this compound's stability and compatibility with a wide range of reaction conditions make it a valuable tool for synthetic chemists aiming to explore new synthetic routes and develop novel compounds with diverse applications.