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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, [(1S)-2-iodo-1-methylethyl]-, phenylmethyl ester

IC[C@@H](NC(=O)OCc1ccccc1)C Request for Quotation
Chemical Name: Carbamic acid, [(1S)-2-iodo-1-methylethyl]-, phenylmethyl ester
CAS Number: 136464-11-4
Product Number: AG0011VP(AGN-PC-0O1A5U)
Synonyms:
MDL No:
Molecular Formula: C11H14INO2
Molecular Weight: 319.1388

Identification/Properties

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


(S)-Benzyl (1-iodopropan-2-yl)carbamate is a versatile compound that finds extensive application in chemical synthesis. Due to its unique structure and reactivity, this compound serves as a valuable building block in the synthesis of various organic compounds. One key application of (S)-Benzyl (1-iodopropan-2-yl)carbamate is as a chiral auxiliary in asymmetric synthesis. By utilizing its chiral nature, this compound can facilitate the formation of enantiomerically pure products, making it a valuable tool for the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, (S)-Benzyl (1-iodopropan-2-yl)carbamate can be used in the synthesis of complex molecules by enabling selective transformations and increasing overall synthetic efficiency. Its strategic incorporation into synthetic routes allows for the creation of highly functionalized compounds with precise stereochemistry, making it an indispensable reagent in modern organic synthesis.