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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 8-amino-1,3,4,5-tetrahydro-2-benzazepine-2-carboxylate

Nc1ccc2c(c1)CN(CCC2)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 8-amino-1,3,4,5-tetrahydro-2-benzazepine-2-carboxylate
CAS Number: 939043-41-1
Product Number: AG00GXVI(AGN-PC-0D5PRU)
Synonyms:
MDL No:
Molecular Formula: C15H22N2O2
Molecular Weight: 262.3474

Identification/Properties

Computed Properties
Molecular Weight:
262.353g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
262.168g/mol
Monoisotopic Mass:
262.168g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
325
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H312-H332
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 8-amino-4,5-dihydro-1H-benzo[c]azepine-2(3H)-carboxylate plays a vital role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable precursor in the preparation of various heterocyclic compounds and pharmaceutical intermediates. This compound is particularly utilized in the synthesis of complex molecules due to its ability to introduce the tert-butyl group as a protective group, providing stereochemical control and enhancing the overall yield of the desired products. Additionally, the presence of the amino group allows for further functionalization and diversification of the molecule through a variety of synthetic transformations, making it a valuable tool in organic chemistry research and drug development.