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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)-

Cyclohexanepropanoic acid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-,methyl ester, (aS)-

COC(=O)[C@@H](NC(=O)OC(C)(C)C)CC1CCCCC1 Request for Quotation
Chemical Name: Cyclohexanepropanoic acid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-,methyl ester, (aS)-
CAS Number: 98105-41-0
Product Number: AG003OG1(AGN-PC-0W7VIS)
Synonyms:
MDL No:
Molecular Formula: C15H27NO4
Molecular Weight: 285.3792

Identification/Properties

Properties
MP:
47-49 °C(lit.)
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
285.384g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
285.194g/mol
Monoisotopic Mass:
285.194g/mol
Topological Polar Surface Area:
64.6A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
329
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:
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

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Chemical Structure


(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoate, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. It serves as a key intermediate in the preparation of various pharmaceutical compounds and organic molecules. This compound is widely utilized in the synthesis of bioactive molecules due to its unique structural features and reactivity.In chemical synthesis, (S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoate is commonly employed as a chiral auxiliary or a protecting group. Its chiral nature imparts stereochemical control during reactions, enabling the synthesis of enantiomerically pure compounds. By selectively masking functional groups, this compound facilitates the manipulation of chemical reactivity and the isolation of specific reaction products.Furthermore, (S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoate acts as a valuable precursor for the synthesis of cyclic compounds, heterocycles, and complex natural products. Its ability to undergo various transformations, including deprotection, functional group manipulation, and stereospecific reactions, makes it an indispensable tool in the organic chemist's toolkit.In summary, the application of (S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoate in chemical synthesis offers a wide range of possibilities for the construction of intricate molecular structures, making it an essential component in the development of new drugs, agrochemicals, and materials.