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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)-

Carbamic acid, (trans-4-hydroxycyclohexyl)-, 1,1-dimethylethyl ester

O[C@@H]1CC[C@H](CC1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: Carbamic acid, (trans-4-hydroxycyclohexyl)-, 1,1-dimethylethyl ester
CAS Number: 111300-06-2
Product Number: AG0034K7(AGN-PC-0NXMG9)
Synonyms:
MDL No: MFCD03844613
Molecular Formula: C11H21NO3
Molecular Weight: 215.2893

Identification/Properties

Properties
MP:
172-173°C
BP:
337.7°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
215.293g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
215.152g/mol
Monoisotopic Mass:
215.152g/mol
Topological Polar Surface Area:
58.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
214
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Trans-4-Boc-Aminocyclohexanol, also known as N-tert-butoxycarbonyl-4-aminocyclohexanol, is a versatile compound commonly used in chemical synthesis. This compound plays a crucial role as a protecting group in organic synthesis, particularly in the field of peptide and pharmaceutical chemistry. When utilized in chemical reactions, trans-4-Boc-Aminocyclohexanol can shield specific functional groups in a molecule, preventing undesired reactions from occurring at those sites. This protection is essential for controlling the regioselectivity and stereochemistry of the final product. By selectively deprotecting the Boc group under controlled conditions, chemists can unveil the desired functional groups at the precise timing, leading to the formation of complex molecular structures with high purity and efficiency.Moreover, trans-4-Boc-Aminocyclohexanol serves as a crucial building block for the synthesis of various pharmaceuticals, bioactive compounds, and natural products. Its presence enables chemists to introduce the amino alcohol functionality into target molecules with precision, opening up pathways for the creation of novel drugs and therapeutic agents.In summary, the application of trans-4-Boc-Aminocyclohexanol in chemical synthesis is indispensable for protecting reactive functional groups, controlling reaction pathways, and facilitating the efficient construction of complex molecules with specific biological activities.