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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)-

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

NC[C@@H]1CCN(C1)C(=O)OC(C)(C)C.Cl Request for Quotation
Chemical Name: (S)-1-Boc-3-AMinoMethylpyrrolidine-HCl
CAS Number: 916214-30-7
Product Number: AG006FLV(AGN-PC-0WA2TK)
Synonyms:
MDL No:
Molecular Formula: C10H21ClN2O2
Molecular Weight: 236.7389

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
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-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


(S)-1-Boc-3-Aminomethylpyrrolidine hydrochloride is a versatile chemical reagent commonly used in organic synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials. Its chiral nature makes it particularly useful in asymmetric synthesis, where the stereochemistry of the final product is crucial. By incorporating (S)-1-Boc-3-Aminomethylpyrrolidine hydrochloride into chemical reactions, chemists can selectively form complex molecules with high enantiomeric purity, opening up new possibilities for drug discovery and material science.