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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)-

2,6-Diaminophenol hydrochloride

Nc1cccc(c1O)N.Cl Request for Quotation
Chemical Name: 2,6-Diaminophenol hydrochloride
CAS Number: 1808091-49-7
Product Number: AG0022D7(AGN-PC-0WAMB5)
Synonyms:
MDL No:
Molecular Formula: C6H9ClN2O
Molecular Weight: 160.6015

Identification/Properties

Computed Properties
Molecular Weight:
160.601g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
160.04g/mol
Monoisotopic Mass:
160.04g/mol
Topological Polar Surface Area:
72.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
87.1
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:
2
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


2,6-Diaminophenol hydrochloride is a versatile compound often utilized in chemical synthesis due to its unique properties and reactivity. This compound serves as a crucial building block in the production of various chemicals and materials, particularly in the field of organic chemistry.One of the key applications of 2,6-Diaminophenol hydrochloride in chemical synthesis is its role as a precursor in the synthesis of polymeric materials. By undergoing specific chemical reactions, this compound can be incorporated into polymer chains, imparting desired properties such as thermal stability, mechanical strength, and chemical resistance to the final material.Additionally, 2,6-Diaminophenol hydrochloride is commonly employed in the synthesis of dyes and pigments. Through controlled chemical reactions, this compound can be transformed into colorful molecules that exhibit specific light-absorbing and light-reflecting properties. These dyes and pigments find wide applications in industries such as textiles, printing, and cosmetics.Furthermore, 2,6-Diaminophenol hydrochloride can be utilized in the production of pharmaceutical intermediates. By reacting with other compounds, this versatile building block can be incorporated into drug molecules, facilitating the synthesis of important pharmaceuticals with specific biological activities.Overall, the application of 2,6-Diaminophenol hydrochloride in chemical synthesis enables the creation of diverse materials, dyes, pigments, and pharmaceuticals, showcasing its significance in the realm of organic chemistry.