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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)-

Benzonitrile, 2-amino-3-methoxy-

COc1cccc(c1N)C#N Request for Quotation
Chemical Name: Benzonitrile, 2-amino-3-methoxy-
CAS Number: 148932-68-7
Product Number: AG00AC55(AGN-PC-00GT4Y)
Synonyms:
MDL No:
Molecular Formula: C8H8N2O
Molecular Weight: 148.1619

Identification/Properties

Properties
BP:
286.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
148.165g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
148.064g/mol
Monoisotopic Mass:
148.064g/mol
Topological Polar Surface Area:
59A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
172
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-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The organic compound Benzonitrile, 2-amino-3-methoxy-, serves as a valuable building block in chemical synthesis processes. Its incorporation in reactions can lead to the creation of various pharmaceutical intermediates and specialty chemicals due to its unique chemical properties. Benzonitrile, 2-amino-3-methoxy-, can be utilized in the synthesis of heterocyclic compounds, such as pyrazoles and indazoles, through multi-step organic transformations. Additionally, this compound can act as a key precursor in the production of fine chemicals with distinct applications in the pharmaceutical and agrochemical industries. Its strategic placement of functional groups allows for selective modifications and the generation of diverse molecular structures, making it an essential component in the development of novel compounds with potential therapeutic or industrial significance.