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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-(2,3-dihydro-1H-indol-7-yl)carbamate

O=C(OC(C)(C)C)Nc1cccc2c1NCC2 Request for Quotation
Chemical Name: tert-butyl N-(2,3-dihydro-1H-indol-7-yl)carbamate
CAS Number: 885270-12-2
Product Number: AG00486H(AGN-PC-09T63U)
Synonyms:
MDL No:
Molecular Formula: C13H18N2O2
Molecular Weight: 234.2942

Identification/Properties

Computed Properties
Molecular Weight:
234.299g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
234.137g/mol
Monoisotopic Mass:
234.137g/mol
Topological Polar Surface Area:
50.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
286
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 indolin-7-ylcarbamate is a versatile compound that finds wide utility in chemical synthesis. Its unique structure and reactivity make it an invaluable tool for organic chemists in various transformations and reactions.One key application of tert-Butyl indolin-7-ylcarbamate is as a protecting group in peptide synthesis. By selectively shielding specific functional groups on amino acids with this compound, chemists can control the reactivity of the amino acids and prevent unwanted side reactions during the peptide assembly process. The tert-Butyl indolin-7-ylcarbamate can be easily removed under mild conditions after the desired chemical transformations have taken place, allowing for the efficient synthesis of complex peptides and proteins.Additionally, tert-Butyl indolin-7-ylcarbamate can also serve as a useful intermediate in the construction of various heterocyclic compounds. Its presence can facilitate cyclization reactions and lead to the formation of novel structures with diverse applications in medicinal chemistry, material science, and other fields.Overall, the tert-Butyl indolin-7-ylcarbamate represents a valuable building block in the toolbox of synthetic chemists, offering a range of opportunities for the efficient and controlled synthesis of complex organic molecules.