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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)-

D-Proline, 1,1-dimethylethyl ester, hydrochloride

O=C([C@H]1CCCN1)OC(C)(C)C.Cl Request for Quotation
Chemical Name: D-Proline, 1,1-dimethylethyl ester, hydrochloride
CAS Number: 184719-80-0
Product Number: AG003CC5(AGN-PC-0O5BJS)
Synonyms:
MDL No:
Molecular Formula: C9H18ClNO2
Molecular Weight: 207.6977

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Refractive Index:
31 ° (C=1, H2O)
Computed Properties
Molecular Weight:
207.698g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
207.103g/mol
Monoisotopic Mass:
207.103g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
172
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


D-Proline, 1,1-dimethylethyl ester, hydrochloride (1:1) is a versatile compound used in chemical synthesis for various applications. Its unique chemical properties make it a valuable reagent in the production of pharmaceuticals, agrochemicals, and specialty chemicals.This compound serves as a crucial building block in peptide synthesis, particularly in the formation of peptide bonds. Its proline moiety imparts stereochemical constraints that influence the overall conformation of peptides, making it highly desirable in the creation of structurally diverse peptides. Additionally, the presence of the 1,1-dimethylethyl ester group provides protection for sensitive functional groups during the synthetic process.In organic synthesis, D-Proline, 1,1-dimethylethyl ester, hydrochloride (1:1) is employed as a catalyst in various asymmetric transformations. Its ability to act as a chiral auxiliary or organocatalyst enables the selective formation of enantiomerically enriched compounds, which are crucial in the development of pharmaceuticals and fine chemicals.Furthermore, this compound finds application in the preparation of complex natural products and bioactive molecules. Its reactivity and selectivity play a key role in facilitating challenging transformations and enhancing the efficiency of chemical reactions, making it an indispensable tool for synthetic chemists.