1. Home
  2. 5-bromo-2-hydroxy-3-methylbenzonitrile

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

5-bromo-2-hydroxy-3-methylbenzonitrile

N#Cc1cc(Br)cc(c1O)C Request for Quotation
Chemical Name: 5-bromo-2-hydroxy-3-methylbenzonitrile
CAS Number: 913191-20-5
Product Number: AG00H22F(AGN-PC-07B6DT)
Synonyms:
MDL No:
Molecular Formula: C8H6BrNO
Molecular Weight: 212.0433

Identification/Properties

Computed Properties
Molecular Weight:
212.046g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
210.963g/mol
Monoisotopic Mass:
210.963g/mol
Topological Polar Surface Area:
44A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
186
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


5-Bromo-2-hydroxy-3-methylbenzonitrile is a versatile compound that finds wide applications in chemical synthesis. One of the key uses of this compound is as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure makes it valuable in the creation of complex molecules through selective functional group transformations. Additionally, its bromine substituent can serve as a handle for further derivatization, allowing for the introduction of other functional groups with precision. In the realm of medicinal chemistry, 5-Bromo-2-hydroxy-3-methylbenzonitrile can be employed in the construction of biologically active compounds, making it an important tool for drug discovery and development efforts. Its presence in the arsenal of synthetic chemists highlights its significance in the creation of new molecules with diverse applications.