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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-(2-bromoethyl)pyrrolidine-1-carboxylate

BrCCC1CCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 3-(2-bromoethyl)pyrrolidine-1-carboxylate
CAS Number: 958026-66-9
Product Number: AG00IJGC(AGN-PC-0C31IX)
Synonyms:
MDL No:
Molecular Formula: C11H20BrNO2
Molecular Weight: 278.1860

Identification/Properties

Computed Properties
Molecular Weight:
278.19g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
277.068g/mol
Monoisotopic Mass:
277.068g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
225
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-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


tert-Butyl 3-(2-bromoethyl)pyrrolidine-1-carboxylate is a versatile compound that finds wide application in chemical synthesis. This compound serves as a valuable building block in organic chemistry for the preparation of various complex molecules. Its unique structure, characterized by the presence of a pyrrolidine ring and a tert-butyl ester group, enables it to participate in a range of chemical reactions.In organic synthesis, tert-Butyl 3-(2-bromoethyl)pyrrolidine-1-carboxylate can be used for the introduction of the pyrrolidine scaffold into target molecules. The presence of the bromoethyl functional group provides a handle for further derivatization through nucleophilic substitution reactions. This allows for the introduction of various substituents or functional groups at the bromine position, thereby facilitating the synthesis of diverse compounds.Furthermore, the tert-butyl ester group in this compound serves as a protecting group for the carboxylic acid moiety. By selectively removing this protecting group under mild conditions, the carboxylic acid functionality can be revealed, enabling further elaboration of the molecule through various synthetic transformations.Overall, tert-Butyl 3-(2-bromoethyl)pyrrolidine-1-carboxylate plays a crucial role in chemical synthesis by offering synthetic chemists a versatile tool for the construction of complex molecular architectures with strategic control over functional group manipulation and stereochemistry.