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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-tert-butyl 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate

COC(=O)C1CC(CN1C(=O)OC(C)(C)C)O Request for Quotation
Chemical Name: 1-tert-butyl 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate
CAS Number: 897046-42-3
Product Number: AG00H2U4(AGN-PC-0WANQ3)
Synonyms:
MDL No: MFCD04115496
Molecular Formula: C11H19NO5
Molecular Weight: 245.2723

Identification/Properties

Computed Properties
Molecular Weight:
245.275g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
245.126g/mol
Monoisotopic Mass:
245.126g/mol
Topological Polar Surface Area:
76.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
310
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


1-(tert-Butyl) 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate serves as a valuable building block in chemical synthesis due to its unique structure and reactivity. This compound can be employed in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its structural features make it a versatile intermediate for the construction of complex organic molecules through a range of synthetic methods. The presence of the tert-butyl group provides steric hindrance, influencing the regioselectivity and stereochemistry of reactions. The 2-methyl substituent adds to the compound's diversity by enabling further functionalization at this position. Additionally, the presence of the hydroxyl group and dicarboxylate moiety offers opportunities for derivatization and the introduction of additional functionality, enhancing the compound's utility in synthetic pathways. Overall, 1-(tert-Butyl) 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate plays a crucial role in the development of novel chemical entities with potential applications across various industries.