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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)-TERT-BUTYL 2-(METHYLAMINO)PROPANOATE HCL

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Chemical Name: (R)-TERT-BUTYL 2-(METHYLAMINO)PROPANOATE HCL
CAS Number: 1314999-27-3
Product Number: AG01DMGK(AG01DMGK)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


N-Me-D-Ala-OtBu hydrochloride serves as a versatile building block in chemical synthesis due to its specific properties and reactivity. As a protected form of N-methyl-D-alanine, this compound provides a convenient means to introduce the N-methyl-D-alanine moiety into various organic molecules. It can participate in peptide synthesis, drug development, and other related applications by acting as a key intermediate in the creation of complex structures. Additionally, the t-butoxycarbonyl (Boc) protecting group enhances the stability of the N-Me-D-Ala-OtBu hydrochloride, allowing for controlled manipulation and selective deprotection during synthetic processes. Its unique combination of structural features makes it a valuable tool for chemists seeking to access diverse molecular architectures and functional groups.