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  2. Benzeneacetic acid, a,4-dihydroxy-, hydrate (1:1)OTHER CA INDEX NAMES:Benzeneacetic acid, a,4-dihydroxy-, monohydrate

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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)-

Benzeneacetic acid, a,4-dihydroxy-, hydrate (1:1)OTHER CA INDEX NAMES:Benzeneacetic acid, a,4-dihydroxy-, monohydrate

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Chemical Name: Benzeneacetic acid, a,4-dihydroxy-, hydrate (1:1)OTHER CA INDEX NAMES:Benzeneacetic acid, a,4-dihydroxy-, monohydrate
CAS Number: 184901-84-6
Product Number: AG00APS4(AGN-PC-0QDQW5)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
186.163g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
186.053g/mol
Monoisotopic Mass:
186.053g/mol
Topological Polar Surface Area:
78.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
160
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Hydroxy-2-(4-hydroxyphenyl)acetic acid hydrate, also known as dihydroxyphenylacetic acid hydrate, plays a crucial role in chemical synthesis as a versatile building block. With its unique chemical structure, this compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals.Its hydroxyphenyl group provides a reactive site for further functionalization, allowing chemists to modify and tailor the compound for specific applications. In organic synthesis, 2-Hydroxy-2-(4-hydroxyphenyl)acetic acid hydrate is often used in the preparation of biologically active molecules and complex organic compounds. Its presence can enhance the reactivity of an organic reaction and facilitate the formation of desired chemical bonds.Furthermore, this compound can be used as a phenolic building block in the synthesis of polymers and materials with specific properties, such as antioxidant or UV-absorbing characteristics. Its ability to undergo various chemical transformations makes it a valuable tool in the hands of synthetic chemists for designing and creating new molecules with tailored functions and properties.