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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, (2,2-dimethoxyethyl)-, 1,1-dimethylethyl ester

COC(CNC(=O)OC(C)(C)C)OC Request for Quotation
Chemical Name: Carbamic acid, (2,2-dimethoxyethyl)-, 1,1-dimethylethyl ester
CAS Number: 127119-09-9
Product Number: AG000WON(AGN-PC-001NYZ)
Synonyms:
MDL No:
Molecular Formula: C9H19NO4
Molecular Weight: 205.2515

Identification/Properties

Computed Properties
Molecular Weight:
205.254g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
205.131g/mol
Monoisotopic Mass:
205.131g/mol
Topological Polar Surface Area:
56.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
172
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


The tert-butyl (2,2-dimethoxyethyl)carbamate, also known as Boc-DEOC, is a versatile compound commonly used in chemical synthesis. This compound serves as a protecting group, enabling selective protection of amine functionalities in various organic reactions. By reacting with the amine group, Boc-DEOC forms a stable carbamate linkage, effectively preventing unwanted side reactions or unwanted interactions with other functional groups. This protection can be selectively removed under mild conditions, allowing for further modification at the deprotected amine site. The ease of installation and removal makes tert-butyl (2,2-dimethoxyethyl)carbamate a valuable tool in the synthesis of complex organic molecules, pharmaceutical intermediates, and bioactive compounds.