What is the 2,5-DIHYDROXY-4'-METHYLBIPHENYL?

2,5-DIHYDROXY-4'-METHYLBIPHENYL is , while it's Molecular Formula is C13H12 O2. Used in Pharmaceutical Industry: 2,5-Dihydroxy-4'-methylbiphenyl is used as an intermediate in the synthesis of pharmaceuticals for its potential therapeutic applications. Its antioxidant properties and chemical structure make it a valuable component in the development of new drugs. Used in Dye Industry: In the dye industry, 2,5-dihydroxy-4'-methylbiphenyl is used as a precursor in the production of various dyes. Its chemical structure allows for the creation of dyes with specific color properties and stability. Used in Organic Product Synthesis: 2,5-Dihydroxy-4'-methylbiphenyl is utilized as a building block in the synthesis of other organic products, such as specialty chemicals and materials, due to its unique molecular structure and functional groups. Used in Antioxidant Applications: 2,5-Dihydroxy-4'-methylbiphenyl is used as an antioxidant in various applications, including food preservation, cosmetics, and industrial processes. Its antioxidant properties help prevent oxidation and degradation, extending the shelf life and improving the quality of products. Used in Research and Development: In the field of research and development, 2,5-dihydroxy-4'-methylbiphenyl is used as a model compound to study the properties and behavior of biphenyls and their derivatives. This helps in understanding their potential applications and developing new methods for their synthesis and utilization.

What is the CAS number for 2,5-DIHYDROXY-4'-METHYLBIPHENYL?

The CAS number of 2,5-DIHYDROXY-4'-METHYLBIPHENYL is 10551-32-3.

What is 2,5-DIHYDROXY-4'-METHYLBIPHENYL (10551-32-3) used for?

2,5-Dihydroxy-4'-methylbiphenyl, also known as 4'-methyl-2,5-dihydroxybiphenyl, is a chemical compound with the molecular formula C13H12O2. It belongs to the class of biphenyls, which are organic compounds composed of two linked benzene rings. This specific compound features two hydroxyl (OH) groups and a methyl (CH3) group attached to its biphenyl ring structure. Known for its antioxidant properties, 2,5-dihydroxy-4'-methylbiphenyl is utilized in the production of pharmaceuticals, dyes, and other organic products, and is under investigation for its potential therapeutic applications in various medical treatments. However, it is crucial to handle 2,5-DIHYDROXY-4'-METHYLBIPHENYL with care due to potential health risks if not used under controlled conditions.

What is the 2,5-DIHYDROXY-4'-METHYLBIPHENYL?

2,5-DIHYDROXY-4'-METHYLBIPHENYL is , while it's Molecular Formula is C13H12 O2. Used in Pharmaceutical Industry: 2,5-Dihydroxy-4'-methylbiphenyl is used as an intermediate in the synthesis of pharmaceuticals for its potential therapeutic applications. Its antioxidant properties and chemical structure make it a valuable component in the development of new drugs. Used in Dye Industry: In the dye industry, 2,5-dihydroxy-4'-methylbiphenyl is used as a precursor in the production of various dyes. Its chemical structure allows for the creation of dyes with specific color properties and stability. Used in Organic Product Synthesis: 2,5-Dihydroxy-4'-methylbiphenyl is utilized as a building block in the synthesis of other organic products, such as specialty chemicals and materials, due to its unique molecular structure and functional groups. Used in Antioxidant Applications: 2,5-Dihydroxy-4'-methylbiphenyl is used as an antioxidant in various applications, including food preservation, cosmetics, and industrial processes. Its antioxidant properties help prevent oxidation and degradation, extending the shelf life and improving the quality of products. Used in Research and Development: In the field of research and development, 2,5-dihydroxy-4'-methylbiphenyl is used as a model compound to study the properties and behavior of biphenyls and their derivatives. This helps in understanding their potential applications and developing new methods for their synthesis and utilization.

What is the CAS number for 2,5-DIHYDROXY-4'-METHYLBIPHENYL?

The CAS number of 2,5-DIHYDROXY-4'-METHYLBIPHENYL is 10551-32-3.

What is 2,5-DIHYDROXY-4'-METHYLBIPHENYL (10551-32-3) used for?

2,5-Dihydroxy-4'-methylbiphenyl, also known as 4'-methyl-2,5-dihydroxybiphenyl, is a chemical compound with the molecular formula C13H12O2. It belongs to the class of biphenyls, which are organic compounds composed of two linked benzene rings. This specific compound features two hydroxyl (OH) groups and a methyl (CH3) group attached to its biphenyl ring structure. Known for its antioxidant properties, 2,5-dihydroxy-4'-methylbiphenyl is utilized in the production of pharmaceuticals, dyes, and other organic products, and is under investigation for its potential therapeutic applications in various medical treatments. However, it is crucial to handle 2,5-DIHYDROXY-4'-METHYLBIPHENYL with care due to potential health risks if not used under controlled conditions.

Others

Your Location:Home > Others > 2,5-DIHYDROXY-4'-METHYLBIPHENYL

Product classification

Contact us

2,5-DIHYDROXY-4'-METHYLBIPHENYL

CasNo：10551-32-3
purity：99%

Inquiry Add to cart

Details

Factory supply 2,5-DIHYDROXY-4'-METHYLBIPHENYL 10551-32-3 with sufficient production capacity

Molecular Formula: C13H12 O2
Molecular Weight: 200.237
Melting Point: 125°C
Boiling Point: 389.6°Cat760mmHg
Flash Point: 192.7°C
PSA： 40.46000
Density: 1.192g/cm³
LogP: 3.07320

10551-32-3 Relevant articles

Reversible formation of aryloxenium ions from the corresponding quinols under acidic conditions

Chakraborty, Mrinal,Brzozowski, Christopher F.,Novak, Michael

, p. 1236 - 1242 (2012)

Quinols, 1, are products of the hydratio...

Novel access to cyclohexane-1,4-diones and 1,4-hydroquinones via radical 1,2-acyl rearrangement on 2-(halomethyl)cyclopentane-1,3-diones using cobaloxime-mediated electroreduction or tributyltin hydride

Kawafuchi, Hiroyuki,Inokuchi, Tsutomu

, p. 2051 - 2054 (2007/10/03)

A new preparative access to syntheticall...

Acid-catalyzed rearrangement of O-(2-arylphenyl)hydroxylamines to aryldihydroazepinones

Endo, Yasuyuki,Kataoka, Ken-Ichiro,Haga, Naoki,Shudo, Koichi

, p. 3339 - 3342 (2007/10/02)

Acid-catalyzed rearrangement of O-(2-ary...

1,3-Dipolar Cycloaddition Reactions of 1,4-Benzoquinones with Nitrilimines

Argyropoulos, N. G.,Mentzafos, D.,Terzis, A.

, p. 1983 - 1988 (2007/10/02)

The cycloaddition reactions of some aryl...

10551-32-3 Process route

: 583-69-7
2-bromobenzene-1,4-diol

: 5720-05-8
4-methylphenylboronic acid

: 10551-32-3
(4-methylphenyl)-hydroquinone

Conditions

Conditions	Yield
With tetrakis(triphenylphosphine) palladium⁽⁰⁾; water; sodium carbonate; In ethanol; toluene; at 90 ℃; for 24h; Schlenk technique; Inert atmosphere;	55%

: 583-63-1
ortoquinone

: 106-49-0,12221-03-3
p -toluidine

: 10551-32-3
(4-methylphenyl)-hydroquinone

: 30237-07-1
p -tolyl-[1,4]benzoquinone

Conditions

Conditions	Yield
	65%

10551-32-3 Upstream products

30237-07-1
p -tolyl-[1,4]benzoquinone
142835-77-6
O-(4'-Methyl-biphenyl-2-yl)-hydroxylamine
15424-14-3
N-phenylbenzohydrazonoyl chloride
36590-52-0
N-phenyl-p-chlorobenzohydrazonoyl chloride

10551-32-3 Downstream products

30237-07-1
p -tolyl-[1,4]benzoquinone

4-(4-hydroxy-3-methoxyphenyl)butan-2-ol

Halometasone

ALPHA-GLYCEROPHOSPHORIC ACID DISODIUM SALT

3,3'-methylenebis[tetrahydro-2H-1,3-oxazine]

1,3,3-trimethyl-2-[3-[1-methylanilino-4,6-di-p-tolyl-1H-pyridin-2-ylidene]prop-1-enyl]-3H-indolium iodide

Home

About

Our Products

Organic Chemicals

Agrochemicals

Pharmaceutical

Sweeteners

Others

News

Reach Us

Others

Product classification

Contact us

2,5-DIHYDROXY-4'-METHYLBIPHENYL

Details

Factory supply 2,5-DIHYDROXY-4'-METHYLBIPHENYL 10551-32-3 with sufficient production capacity

10551-32-3 Relevant articles

Reversible formation of aryloxenium ions from the corresponding quinols under acidic conditions

Chakraborty, Mrinal,Brzozowski, Christopher F.,Novak, Michael

, p. 1236 - 1242 (2012)

Novel access to cyclohexane-1,4-diones and 1,4-hydroquinones via radical 1,2-acyl rearrangement on 2-(halomethyl)cyclopentane-1,3-diones using cobaloxime-mediated electroreduction or tributyltin hydride

Kawafuchi, Hiroyuki,Inokuchi, Tsutomu

, p. 2051 - 2054 (2007/10/03)

Acid-catalyzed rearrangement of O-(2-arylphenyl)hydroxylamines to aryldihydroazepinones

Endo, Yasuyuki,Kataoka, Ken-Ichiro,Haga, Naoki,Shudo, Koichi

, p. 3339 - 3342 (2007/10/02)

1,3-Dipolar Cycloaddition Reactions of 1,4-Benzoquinones with Nitrilimines

Argyropoulos, N. G.,Mentzafos, D.,Terzis, A.

, p. 1983 - 1988 (2007/10/02)

10551-32-3 Process route

10551-32-3 Upstream products

10551-32-3 Downstream products

Related Products