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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)-

5H-Dibenz[b,f]azepin-10-ol, 10,11-dihydro-

OC1Cc2ccccc2Nc2c1cccc2 Request for Quotation
Chemical Name: 5H-Dibenz[b,f]azepin-10-ol, 10,11-dihydro-
CAS Number: 4014-77-1
Product Number: AG00D5X9(AGN-PC-0JJ64J)
Synonyms:
MDL No:
Molecular Formula: C14H13NO
Molecular Weight: 211.2591

Identification/Properties

Computed Properties
Molecular Weight:
211.264g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
211.1g/mol
Monoisotopic Mass:
211.1g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
243
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


10,11-Dihydro-5H-dibenzo[b,f]azepin-10-ol is a versatile compound that finds application in various chemical synthesis processes. As a key building block in organic chemistry, it serves as a valuable intermediate for the synthesis of complex molecules. Its unique structure and reactivity make it an important tool for creating new compounds with diverse functionalities.In chemical synthesis, 10,11-Dihydro-5H-dibenzo[b,f]azepin-10-ol can be utilized as a precursor in the formation of heterocyclic compounds, pharmaceuticals, and agrochemicals. Its presence in a reaction mixture can lead to the formation of fused ring systems, allowing for the creation of molecules with specific properties and biological activities.Furthermore, this compound can participate in various transformations such as oxidation, reduction, and functional group manipulation. Its role as a scaffold in synthetic pathways enables chemists to access a wide range of structurally complex molecules efficiently.Overall, 10,11-Dihydro-5H-dibenzo[b,f]azepin-10-ol is a valuable tool in chemical synthesis, offering chemists the opportunity to construct novel compounds and explore new avenues in organic chemistry research.