1. Home
  2. Carbamic acid, (4-hydroxycyclohexyl)-, 1,1-dimethylethyl ester

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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, (4-hydroxycyclohexyl)-, 1,1-dimethylethyl ester

OC1CCC(CC1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: Carbamic acid, (4-hydroxycyclohexyl)-, 1,1-dimethylethyl ester
CAS Number: 224309-64-2
Product Number: AG003KAH(AGN-PC-0K6A42)
Synonyms:
MDL No: MFCD06658349
Molecular Formula: C11H21NO3
Molecular Weight: 215.2893

Identification/Properties

Properties
MP:
170.0 to 174.0 °C
BP:
337.7°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The tert-Butyl (4-hydroxycyclohexyl)carbamate compound serves as a versatile reagent in chemical synthesis, specifically in the field of organic synthesis. This molecule plays a crucial role in the protection of hydroxyl groups in various organic compounds, offering a method for selectively shielding hydroxyl functionalities for further manipulation and control in multi-step synthesis processes. By employing tert-Butyl (4-hydroxycyclohexyl)carbamate, chemists can safeguard hydroxyl moieties during reactions that may otherwise lead to undesired side reactions or unwanted modifications, ultimately enabling the targeted synthesis of complex organic molecules with precision and efficiency. Furthermore, this compound's stability and compatibility with a wide range of reaction conditions make it a valuable tool for chemists seeking to streamline synthetic routes and achieve high-yield transformations in the laboratory.