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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)-

Ethyl trans-2-[4-(Boc-amino)cyclohexyl]acetate

CCOC(=O)C[C@@H]1CC[C@H](CC1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: Ethyl trans-2-[4-(Boc-amino)cyclohexyl]acetate
CAS Number: 946598-34-1
Product Number: AG00IIFA(AGN-PC-0WAD9Q)
Synonyms:
MDL No: MFCD20491405
Molecular Formula: C15H27NO4
Molecular Weight: 285.3792

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 2-(trans-4-((tert-butoxycarbonyl)amino)cyclohexyl)acetate is a versatile compound with significant application in chemical synthesis, particularly in the field of organic chemistry. This compound is commonly utilized as a key intermediate in the synthesis of various complex organic molecules due to its unique structural properties.In chemical synthesis, Ethyl 2-(trans-4-((tert-butoxycarbonyl)amino)cyclohexyl)acetate serves as a valuable building block for the creation of diverse pharmaceuticals, agrochemicals, and functional materials. Its specific structure enables it to participate in various reactions, such as esterification, amidation, and hydrogenation, allowing for the efficient production of target molecules.Furthermore, the presence of the tert-butoxycarbonyl (Boc) protecting group in Ethyl 2-(trans-4-((tert-butoxycarbonyl)amino)cyclohexyl)acetate provides strategic control over the reactivity of the compound, facilitating selective transformations during the synthesis process. This feature is particularly advantageous in the synthesis of complex molecules where specific functional groups need to be protected or selectively modified.Overall, Ethyl 2-(trans-4-((tert-butoxycarbonyl)amino)cyclohexyl)acetate plays a crucial role in chemical synthesis by enabling the construction of intricate organic structures with high efficiency and selectivity. Its broad utility and compatibility with various synthetic methodologies make it a valuable tool for chemists engaged in the development of novel compounds for diverse applications.