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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)-Benzyl 2-(hydroxymethyl)piperazine-1-carboxylate

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Chemical Name: (S)-Benzyl 2-(hydroxymethyl)piperazine-1-carboxylate
CAS Number: 1217675-92-7
Product Number: AG00HGDW(AGN-PC-0WD2D4)
Synonyms:
MDL No: MFCD09954312
Molecular Formula:
Molecular Weight:

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-Benzyl 2-(hydroxymethyl)piperazine-1-carboxylate is a versatile compound that finds valuable application in chemical synthesis processes. This compound is utilized as a key intermediate in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it a crucial building block for the synthesis of complex molecules in the laboratory.The (S)-Benzyl 2-(hydroxymethyl)piperazine-1-carboxylate plays a significant role in organic synthesis due to its ability to participate in a wide range of chemical reactions, including nucleophilic substitution, acylation, and amide bond formation. Chemists often leverage its structural features to introduce specific functional groups or stereochemical configurations into target molecules, thus enabling the design and production of novel compounds with desired properties.Furthermore, the (S)-Benzyl 2-(hydroxymethyl)piperazine-1-carboxylate can serve as a chiral auxiliary, facilitating asymmetric synthesis by controlling the stereochemistry of certain reactions. This compound's versatility and compatibility with various synthetic methodologies make it a valuable tool for chemists working in medicinal chemistry, materials science, and other fields requiring the precise manipulation of molecular structures.