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  2. tert-butyl N-methyl-N-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]carbamate

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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-methyl-N-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]carbamate

O=C(N(Cc1ccc(cc1)B1OC(C(O1)(C)C)(C)C)C)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl N-methyl-N-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]carbamate
CAS Number: 936728-17-5
Product Number: AG00H32O(AGN-PC-0CSZNK)
Synonyms:
MDL No:
Molecular Formula: C19H30BNO4
Molecular Weight: 347.2568

Identification/Properties

Computed Properties
Molecular Weight:
347.3g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
347.226789g/mol
Monoisotopic Mass:
347.226789g/mol
Topological Polar Surface Area:
48Ų
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
462
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 methyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)carbamate plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly utilized as a protecting group in organic synthesis due to its stability under a variety of reaction conditions. By selectively masking reactive functional groups with this carbamate, chemists can control the reactivity of specific sites within complex molecules, allowing for the sequential and controlled manipulation of molecular structures. Additionally, the presence of the dioxaborolane moiety provides a convenient handle for subsequent cross-coupling reactions, enabling the efficient introduction of diverse functional groups. This compound's compatibility with a wide range of synthetic methodologies makes it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.