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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-Pyrrolidinecarboxylic acid, 3-methylene-, 1,1-dimethylethyl ester

C=C1CCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-Pyrrolidinecarboxylic acid, 3-methylene-, 1,1-dimethylethyl ester
CAS Number: 114214-71-0
Product Number: AG000ASX(AGN-PC-00OTJE)
Synonyms:
MDL No:
Molecular Formula: C10H17NO2
Molecular Weight: 183.2475

Identification/Properties

Computed Properties
Molecular Weight:
183.251g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
183.126g/mol
Monoisotopic Mass:
183.126g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
228
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 3-methylenepyrrolidine-1-carboxylate is a versatile compound that finds extensive application in modern chemical synthesis processes. Its unique structural characteristics make it a valuable building block for the construction of complex organic molecules and pharmaceutical intermediates.This compound serves as a key reagent in the synthesis of various molecules due to its ability to act as a nucleophile or an electrophile in different reaction conditions. Its tert-butyl group provides steric hindrance, allowing for selective reactions and control over regiochemistry in the formation of new bonds.In organic synthesis, tert-Butyl 3-methylenepyrrolidine-1-carboxylate is commonly used in the preparation of heterocyclic compounds, natural product derivatives, and biologically active molecules. Its presence can enhance the efficiency of reactions such as cycloadditions, C-C bond formations, and functional group transformations.Moreover, this compound's stability and reactivity profile make it a preferred choice for chemists working on the design and synthesis of complex organic molecules with specific structural requirements. Its role in chemical synthesis extends to the development of novel materials, pharmaceuticals, and agrochemicals, highlighting its significance in advancing various scientific fields.