What is the 2,2'-Biphenol?

2,2'-Biphenol is Beige to greyish-beige powder, while it's Molecular Formula is C12H10O2. Beige to greyish-beige powder 2,2'-Dihydroxybiphenyl, is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.

What is the CAS number for 2,2'-Biphenol?

The CAS number of 2,2'-Biphenol is 1806-29-7.

What is 2,2'-Biphenol (1806-29-7) used for?

2,2'-Biphenol, also known as 2,2'-Dihydroxybiphenyl, is a member of the hydroxybiphenyls class, characterized by the presence of hydroxy groups at positions 2 and 2'. It appears as a beige to greyish-beige powder and serves as a crucial raw material and intermediate in various industries.

What is the 2,2'-Biphenol?

2,2'-Biphenol is Beige to greyish-beige powder, while it's Molecular Formula is C12H10O2. Beige to greyish-beige powder 2,2'-Dihydroxybiphenyl, is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.

What is the CAS number for 2,2'-Biphenol?

The CAS number of 2,2'-Biphenol is 1806-29-7.

What is 2,2'-Biphenol (1806-29-7) used for?

2,2'-Biphenol, also known as 2,2'-Dihydroxybiphenyl, is a member of the hydroxybiphenyls class, characterized by the presence of hydroxy groups at positions 2 and 2'. It appears as a beige to greyish-beige powder and serves as a crucial raw material and intermediate in various industries.

Product classification

Featured Products

2,2'-Bipyridine

Product Name: 2,2'-Bipyridine
CasNo: 1806-29-7
Purity:
Appearance: Beige to greyish-beige powder

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CasNo： 1806-29-7

Molecular Formula： C₁₂H₁₀O₂

Appearance： Beige to greyish-beige powder

Buy Quality Chinese Manufacturer Supply 2,2'-Bipyridine 1806-29-7 with Cheapest Price

Molecular Formula:C12H10O2
Molecular Weight:186.21
Appearance/Colour:Beige to greyish-beige powder
Melting Point:108-110 °C
Refractive Index:1.6086 (estimate)
Boiling Point:314.999 °C at 760 mmHg
PKA:7.32±0.10(Predicted)
Flash Point:160.803 °C
PSA：40.46000
Density:1.228 g/cm³
LogP:2.76480

1806-29-7 Relevant articles

Products, rates, and mechanism of the gas-phase condensation of phenoxy radicals between 500-840 K

Wiater, Izabela,Born, Jan G. P.,Louw, Robert

, p. 921 - 928 (2000)

Phenols are demonstrated precursors of '...

THE ROLE OF STEREOELECTRONIC FACTORS IN THE OXIDATION OF PHENOLS

Armstrong, David R.,Breckenridge, Robin J.,Cameron, Colin,Nonhebel, Derek C.,Pauson, Peter L.,Perkins, Peter G.

, p. 1071 - 1074 (1983)

The oxidative coupling of both 3,5-dimet...

Synthesis of the spirocyclic cyclohexadienone ring system of the schiarisanrins.

Coleman,Guernon,Roland

, p. 277 - 280 (2000)

[structure: see text] Studies on the syn...

-

Britton,zit. bei Gilman,Swiss,Cheney

, p. 1963,1964 (1940)

CuO grafted triazine functionalized covalent organic framework as an efficient catalyst for C-C homo coupling reaction

Das, Sabuj Kanti,Krishna Chandra, Bijan,Molla, Rostam A.,Sengupta, Manideepa,Islam, Sk. Manirul,Majee, Adinath,Bhaumik, Asim

, (2020)

Designing of low cost catalytic system f...

Photochemistry of Dibenzo-1,4-dioxin: Formation of 2,2'-Biphenylquinone as an Observable Intermediate

Guan, Bing,Wan, Peter

, p. 409 - 410 (1993)

Photolysis of dibenzo-1,4-dioxin 1, whic...

Photochemical rearrangement of chlorinated dibenzo-p-dioxins. Regioselective carbon-oxygen bond homolysis from the singlet excited state, and carbon-chlorine bond homolysis from the triplet excited state

Kobayashi, Takanori,Shimada, Jun-Ichi,Kitahara, Chieko,Haga, Naoki

, p. 348 - 349 (2006)

UV light irradiation of 1-chloro-, 2-chl...

Small Molecule NF-κB Inhibitors as Immune Potentiators for Enhancement of Vaccine Adjuvants

Moser, Brittany A.,Escalante-Buendia, Yoseline,Steinhardt, Rachel C.,Rosenberger, Matthew G.,Cassaidy, Britteny J.,Naorem, Nihesh,Chon, Alfred C.,Nguyen, Minh H.,Tran, Ngoctran T.,Esser-Kahn, Aaron P.

, (2020)

Adjuvants are added to vaccines to enhan...

Phenol conversion and dimeric intermediates in horseradish peroxidase-catalyzed phenol removal from water

Jian Yu,Taylor,Huixian Zou,Biswas,Bewtra

, p. 2154 - 2160 (1994)

Phenol was removed from water by horsera...

SECOND-ORDER COMBINATION REACTION OF PHENOXYL RADICALS

Ye, Mingyu,Schuler, Robert H.

, p. 1898 - 1902 (1989)

Phenoxy radicals, when produced pulse ra...

Dendrimer-encapsulated Pd nanoparticles as aqueous, room-temperature catalysts for the Stille reaction

Garcia-Martinez, Joaquin C.,Lezutekong, Raphael,Crooks, Richard M.

, p. 5097 - 5103 (2005)

We report that dendrimer-encapsulated Pd...

Ir-Catalyzed Ligand-Free Directed C-H Borylation of Arenes and Pharmaceuticals: Detailed Mechanistic Understanding

Mahamudul Hassan, Mirja Md,Mondal, Biplab,Singh, Sukriti,Haldar, Chabush,Chaturvedi, Jagriti,Bisht, Ranjana,Sunoj, Raghavan B.,Chattopadhyay, Buddhadeb

supporting information, p. 4360 - 4375 (2022/03/16)

An efficient method for Ir-catalyzed lig...

A mild and practical method for deprotection of aryl methyl/benzyl/allyl ethers with HPPh2andtBuOK

Pan, Wenjing,Li, Chenchen,Zhu, Haoyin,Li, Fangfang,Li, Tao,Zhao, Wanxiang

, p. 7633 - 7640 (2021/09/22)

A general method for the demethylation, ...

Conversion method of dibenzo[c,e][1,2]oxathiane-6-oxide compound

-

Paragraph 0073; 0075; 0101-0106, (2020/02/04)

The invention relates to the technical f...

1806-29-7 Process route

: 132-64-9,214827-48-2
dibenzofuran

: 1806-29-7
2,2'-dihydroxybiphenyl

Conditions

Conditions	Yield
With potassium hydroxide; sodium hydroxide; at 400 - 410 ℃; im Eisenrohr;
With potassium hydroxide; 9H-carbazole; at 250 - 275 ℃;
With potassium hydroxide; 9H-fluorene; at 250 - 275 ℃;
With indole; potassium hydroxide; at 250 - 275 ℃;
With potassium hydroxide; phenanthrene; at 200 - 230 ℃;

: 4783-30-6
6,6'-dihydroxy-1,1'-biphenyl-3,3'-dicarboxylic acid

: 132-64-9,214827-48-2
dibenzofuran

: 1806-29-7
2,2'-dihydroxybiphenyl

Conditions

Conditions	Yield
With hydrogenchloride; at 270 ℃;

1806-29-7 Upstream products

132-64-9
dibenzofuran
4783-30-6
6,6'-dihydroxy-1,1'-biphenyl-3,3'-dicarboxylic acid
108-95-2
phenol
262-12-4
dioxin

1806-29-7 Downstream products

32750-04-2
3.5.3'.5'-Tetranitro-2.2'-dihydroxy-biphenyl
115101-36-5
2'-Dibenzo[d,f][1,3,2]dioxaphosphepin-6-yloxy-biphenyl-2-ol
856055-34-0
2,5-dihydroxy-3,6-bis-(2'-hydroxy-biphenyl-2-yloxy)-terephthalic acid diethyl ester
25483-66-3
1-(2'-hydroxyphenyl)-2,5-benzoquinone

Organic Chemistry

Product classification

Featured Products

2,2'-Bipyridine

Buy Quality Chinese Manufacturer Supply 2,2'-Bipyridine 1806-29-7 with Cheapest Price

1806-29-7 Relevant articles

Products, rates, and mechanism of the gas-phase condensation of phenoxy radicals between 500-840 K

Wiater, Izabela,Born, Jan G. P.,Louw, Robert

, p. 921 - 928 (2000)

THE ROLE OF STEREOELECTRONIC FACTORS IN THE OXIDATION OF PHENOLS

Armstrong, David R.,Breckenridge, Robin J.,Cameron, Colin,Nonhebel, Derek C.,Pauson, Peter L.,Perkins, Peter G.

, p. 1071 - 1074 (1983)

Synthesis of the spirocyclic cyclohexadienone ring system of the schiarisanrins.

Coleman,Guernon,Roland

, p. 277 - 280 (2000)

-

Britton,zit. bei Gilman,Swiss,Cheney

, p. 1963,1964 (1940)

CuO grafted triazine functionalized covalent organic framework as an efficient catalyst for C-C homo coupling reaction

Das, Sabuj Kanti,Krishna Chandra, Bijan,Molla, Rostam A.,Sengupta, Manideepa,Islam, Sk. Manirul,Majee, Adinath,Bhaumik, Asim

, (2020)

Photochemistry of Dibenzo-1,4-dioxin: Formation of 2,2'-Biphenylquinone as an Observable Intermediate

Guan, Bing,Wan, Peter

, p. 409 - 410 (1993)

Photochemical rearrangement of chlorinated dibenzo-p-dioxins. Regioselective carbon-oxygen bond homolysis from the singlet excited state, and carbon-chlorine bond homolysis from the triplet excited state

Kobayashi, Takanori,Shimada, Jun-Ichi,Kitahara, Chieko,Haga, Naoki

, p. 348 - 349 (2006)

Small Molecule NF-κB Inhibitors as Immune Potentiators for Enhancement of Vaccine Adjuvants

Moser, Brittany A.,Escalante-Buendia, Yoseline,Steinhardt, Rachel C.,Rosenberger, Matthew G.,Cassaidy, Britteny J.,Naorem, Nihesh,Chon, Alfred C.,Nguyen, Minh H.,Tran, Ngoctran T.,Esser-Kahn, Aaron P.

, (2020)

Phenol conversion and dimeric intermediates in horseradish peroxidase-catalyzed phenol removal from water

Jian Yu,Taylor,Huixian Zou,Biswas,Bewtra

, p. 2154 - 2160 (1994)

SECOND-ORDER COMBINATION REACTION OF PHENOXYL RADICALS

Ye, Mingyu,Schuler, Robert H.

, p. 1898 - 1902 (1989)

Dendrimer-encapsulated Pd nanoparticles as aqueous, room-temperature catalysts for the Stille reaction

Garcia-Martinez, Joaquin C.,Lezutekong, Raphael,Crooks, Richard M.

, p. 5097 - 5103 (2005)

Ir-Catalyzed Ligand-Free Directed C-H Borylation of Arenes and Pharmaceuticals: Detailed Mechanistic Understanding

Mahamudul Hassan, Mirja Md,Mondal, Biplab,Singh, Sukriti,Haldar, Chabush,Chaturvedi, Jagriti,Bisht, Ranjana,Sunoj, Raghavan B.,Chattopadhyay, Buddhadeb

supporting information, p. 4360 - 4375 (2022/03/16)

A mild and practical method for deprotection of aryl methyl/benzyl/allyl ethers with HPPh2andtBuOK

Pan, Wenjing,Li, Chenchen,Zhu, Haoyin,Li, Fangfang,Li, Tao,Zhao, Wanxiang

, p. 7633 - 7640 (2021/09/22)

Conversion method of dibenzo[c,e][1,2]oxathiane-6-oxide compound

-

Paragraph 0073; 0075; 0101-0106, (2020/02/04)

1806-29-7 Process route

1806-29-7 Upstream products

1806-29-7 Downstream products

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