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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)-

tert-butyl N-(1-cyano-2-methylpropan-2-yl)carbamate

N#CCC(NC(=O)OC(C)(C)C)(C)C Request for Quotation
Chemical Name: tert-butyl N-(1-cyano-2-methylpropan-2-yl)carbamate
CAS Number: 1378608-46-8
Product Number: AG0013YN(AGN-PC-0GX728)
Synonyms:
MDL No:
Molecular Formula: C10H18N2O2
Molecular Weight: 198.2621

Identification/Properties

Computed Properties
Molecular Weight:
198.266g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
198.137g/mol
Monoisotopic Mass:
198.137g/mol
Topological Polar Surface Area:
62.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
255
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

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


The tert-Butyl (1-cyano-2-methylpropan-2-yl)carbamate is a versatile compound commonly used in chemical synthesis as a protecting group for amines. This compound serves as a valuable tool in organic chemistry by temporarily masking the amino group, providing chemists with control over the reactivity of the amine functionality during various synthetic transformations.By selectively blocking the amine group with the tert-Butyl (1-cyano-2-methylpropan-2-yl)carbamate, chemists can prevent unwanted side reactions and direct the desired chemical reactions towards specific functional groups. This protective group strategy allows for the successful formation of complex molecules by enabling sequential modifications while preserving the amine functionality until needed.In addition, the tert-Butyl (1-cyano-2-methylpropan-2-yl)carbamate offers excellent stability under a wide range of reaction conditions, making it an ideal choice for protecting amines in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its ease of installation and removal, along with its compatibility with various synthetic methodologies, make it a valuable asset in the toolbox of synthetic chemists aiming to construct intricate molecular structures with precision and efficiency.