1. Home
  2. Boc-(R)-4-(2-propynyl)-L-proline

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Boc-(R)-4-(2-propynyl)-L-proline

C#CC[C@@H]1C[C@H](N(C1)C(=O)OC(C)(C)C)C(=O)O Request for Quotation
Chemical Name: Boc-(R)-4-(2-propynyl)-L-proline
CAS Number: 959581-98-7
Product Number: AG00IJNG(AGN-PC-0WAIEU)
Synonyms:
MDL No:
Molecular Formula: C13H19NO4
Molecular Weight: 253.2943

Identification/Properties

Computed Properties
Molecular Weight:
253.298g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
253.131g/mol
Monoisotopic Mass:
253.131g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
388
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The (2S,4R)-1-(tert-Butoxycarbonyl)-4-(prop-2-yn-1-yl)pyrrolidine-2-carboxylic acid, is a versatile compound commonly utilized in chemical synthesis processes. This compound serves as a crucial building block in the creation of various pharmaceuticals, fine chemicals, and organic materials. Its unique structure and properties make it particularly valuable in the formation of complex molecules with specific stereochemistry. When incorporated into synthetic routes, this compound plays a key role in enhancing the overall efficiency and yield of desired products. Specifically, its functional groups enable precise control over reactions, facilitating the generation of diverse molecular structures with high purity. Furthermore, the (2S,4R)-1-(tert-Butoxycarbonyl)-4-(prop-2-yn-1-yl)pyrrolidine-2-carboxylic acid is instrumental in the development of novel compounds for drug discovery and material science applications, highlighting its importance in advancing chemical synthesis methodologies.