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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, [(3-iodophenyl)methyl]-, 1,1-dimethylethyl ester

O=C(OC(C)(C)C)NCc1cccc(c1)I Request for Quotation
Chemical Name: Carbamic acid, [(3-iodophenyl)methyl]-, 1,1-dimethylethyl ester
CAS Number: 263351-43-5
Product Number: AG002SSP(AGN-PC-00DBIK)
Synonyms:
MDL No:
Molecular Formula: C12H16INO2
Molecular Weight: 333.1654

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 3-iodobenzylcarbamate is a valuable reagent utilized in various chemical synthesis processes. With its unique structure and properties, this compound plays a crucial role in the synthesis of complex organic molecules. One of the key applications of tert-Butyl 3-iodobenzylcarbamate is as a versatile building block in the preparation of diverse functionalized compounds through C-C and C-N bond formation reactions. Its high reactivity and compatibility with a range of functional groups make it a preferred choice for chemists working on the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, tert-Butyl 3-iodobenzylcarbamate serves as a valuable precursor for the introduction of the 3-iodobenzyl moiety into target molecules, enabling the development of novel structures with tailored properties and functionalities. Its strategic incorporation in synthetic routes contributes to the efficient and sustainable production of desired compounds with enhanced biological activities or material properties.