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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)-

BOC-6-AMINO-1,2,3,4-TETRAHYDROQUINOLINE

O=C(OC(C)(C)C)Nc1ccc2c(c1)CCCN2 Request for Quotation
Chemical Name: BOC-6-AMINO-1,2,3,4-TETRAHYDROQUINOLINE
CAS Number: 474539-25-8
Product Number: AG00D8I5(AGN-00D8CL)
Synonyms:
MDL No:
Molecular Formula: C14H20N2O2
Molecular Weight: 248.3208

Identification/Properties

Computed Properties
Molecular Weight:
248.326g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
248.152g/mol
Monoisotopic Mass:
248.152g/mol
Topological Polar Surface Area:
50.4A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
299
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl (1,2,3,4-tetrahydroquinolin-6-yl)carbamate is a versatile compound widely used in chemical synthesis for its ability to serve as a protecting group for amines. When incorporated into a molecule, this compound can shield the amine functional group from unwanted reactions or interactions during a synthetic process. By selectively protecting the amine, chemists can control the reactivity of other functional groups present in the molecule, allowing for precise manipulation and modification of the compound. This strategy is particularly valuable in the synthesis of complex organic molecules, where specific reactions need to be carried out without interference from reactive amine groups. The tert-Butyl (1,2,3,4-tetrahydroquinolin-6-yl)carbamate plays a crucial role in facilitating the efficient and reliable synthesis of novel compounds for various applications in pharmaceuticals, materials science, and other fields of chemistry.