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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)-

(R)-1-Boc-3-AMinoMethylpyrrolidine-HCl

NC[C@H]1CCN(C1)C(=O)OC(C)(C)C.Cl Request for Quotation
Chemical Name: (R)-1-Boc-3-AMinoMethylpyrrolidine-HCl
CAS Number: 916214-31-8
Product Number: AG006S6K(AGN-PC-0WA2IJ)
Synonyms:
MDL No:
Molecular Formula: C10H21ClN2O2
Molecular Weight: 236.7389

Identification/Properties

Computed Properties
Molecular Weight:
236.74g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
236.129g/mol
Monoisotopic Mass:
236.129g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
211
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-1-Boc-3-Aminomethylpyrrolidine hydrochloride, also known as Boc-AmpHCl, is a versatile compound commonly used in organic synthesis. It serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. As a chiral amine derivative, Boc-AmpHCl plays a crucial role in the asymmetric synthesis of complex molecules by enabling the introduction of chirality at a specific position within a molecule. This compound is particularly valuable in the development of drug candidates and bioactive molecules due to its ability to influence stereochemistry and improve the efficiency of chemical reactions. Leveraging the reactivity and selectivity of Boc-AmpHCl, chemists can access diverse chemical structures with high purity and enantiomeric control, making it an essential reagent in modern synthetic chemistry.