1. Home
  2. [1,1'-Biphenyl]-2-ol, 3'-nitro-

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)-

[1,1'-Biphenyl]-2-ol, 3'-nitro-

Oc1ccccc1c1cccc(c1)[N+](=O)[O-] Request for Quotation
Chemical Name: [1,1'-Biphenyl]-2-ol, 3'-nitro-
CAS Number: 71022-84-9
Product Number: AG0061J1(AGN-PC-0NJ28J)
Synonyms:
MDL No:
Molecular Formula: C12H9NO3
Molecular Weight: 215.2048

Identification/Properties

Properties
MP:
99.5-100℃
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
215.208g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
215.058g/mol
Monoisotopic Mass:
215.058g/mol
Topological Polar Surface Area:
66A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
251
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


In chemical synthesis, 3'-Nitro-[1,1'-biphenyl]-2-ol serves as a versatile building block for the creation of various organic compounds. This compound can be utilized as a key intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity enable it to participate in a wide range of reactions, leading to the formation of diverse molecular architectures. Whether employed as a nucleophilic coupling partner, a directing group for C-H functionalization, or a precursor for heterocyclic synthesis, 3'-Nitro-[1,1'-biphenyl]-2-ol offers chemists a valuable tool for the strategic design and efficient synthesis of complex molecules.