1. Home
  2. Phenol, 4-amino-2,6-dibromo-

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)-

Phenol, 4-amino-2,6-dibromo-

Nc1cc(Br)c(c(c1)Br)O Request for Quotation
Chemical Name: Phenol, 4-amino-2,6-dibromo-
CAS Number: 609-21-2
Product Number: AG003KOB(AGN-PC-0JL8T6)
Synonyms:
MDL No:
Molecular Formula: C6H5Br2NO
Molecular Weight: 266.9180

Identification/Properties

Properties
MP:
195-196 °C(lit.)
BP:
295.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
1.6400 (estimate)
Computed Properties
Molecular Weight:
266.92g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
266.872g/mol
Monoisotopic Mass:
264.874g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Amino-2,6-dibromophenol, a crucial compound in chemical synthesis, serves as a versatile building block in the creation of various pharmaceuticals and agrochemicals. Its unique molecular structure allows for specific functionalization and modification, making it a valuable intermediate in the production of complex organic molecules. This compound is commonly utilized in the synthesis of dyes, pigments, and corrosion inhibitors, showcasing its significance in diverse industrial applications. Its reactive nature and compatibility with a wide range of reagents make it a popular choice for organic chemists seeking to introduce specific functionalities into their target molecules. With its ability to participate in various chemical reactions, 4-Amino-2,6-dibromophenol offers a wide array of possibilities for the development of novel compounds with tailored properties and applications.