What is the 2-Naphthalenol?

2-Naphthalenol is broken white shiny flakes or white powder, while it's Molecular Formula is C10H8O. broken white shiny flakes or white powder Used in Fragrance Industry: 2-Naphthalenol is used as a fragrance ingredient for its distinctive sweet, floral scent, contributing to the production of perfumes, soaps, and other cosmetic products. Its ability to impart a pleasant aroma makes it a valuable component in the creation of various scented products. Used in Chemical Synthesis: 2-Naphthalenol serves as a chemical intermediate in the synthesis of other compounds, including insecticides and pharmaceuticals. Its role in the production of these compounds highlights its importance in the chemical industry and its contribution to the development of various consumer and industrial products. Safety Considerations: While 2-Naphthalenol is not considered to be highly toxic, it can cause irritation to the skin, eyes, and respiratory system upon exposure. Therefore, it is crucial to handle and store this chemical with care to prevent any potential health and safety risks, ensuring the well-being of individuals involved in its production, use, and disposal.

What is the CAS number for 2-Naphthalenol?

The CAS number of 2-Naphthalenol is 135-19-3.

What is 2-Naphthalenol (135-19-3) used for?

2-Naphthalenol, also known as β-naphthol, is a white crystalline compound characterized by a strong, sweet, floral odor. It is derived from naphthalene and is recognized for its versatile applications in various industries due to its unique chemical properties.InChI:InChI=1/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H

What is the 2-Naphthalenol?

2-Naphthalenol is broken white shiny flakes or white powder, while it's Molecular Formula is C10H8O. broken white shiny flakes or white powder Used in Fragrance Industry: 2-Naphthalenol is used as a fragrance ingredient for its distinctive sweet, floral scent, contributing to the production of perfumes, soaps, and other cosmetic products. Its ability to impart a pleasant aroma makes it a valuable component in the creation of various scented products. Used in Chemical Synthesis: 2-Naphthalenol serves as a chemical intermediate in the synthesis of other compounds, including insecticides and pharmaceuticals. Its role in the production of these compounds highlights its importance in the chemical industry and its contribution to the development of various consumer and industrial products. Safety Considerations: While 2-Naphthalenol is not considered to be highly toxic, it can cause irritation to the skin, eyes, and respiratory system upon exposure. Therefore, it is crucial to handle and store this chemical with care to prevent any potential health and safety risks, ensuring the well-being of individuals involved in its production, use, and disposal.

What is the CAS number for 2-Naphthalenol?

The CAS number of 2-Naphthalenol is 135-19-3.

What is 2-Naphthalenol (135-19-3) used for?

2-Naphthalenol, also known as β-naphthol, is a white crystalline compound characterized by a strong, sweet, floral odor. It is derived from naphthalene and is recognized for its versatile applications in various industries due to its unique chemical properties.InChI:InChI=1/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H

Product classification

Featured Products

2-Naphthol

Product Name: 2-Naphthol
CasNo: 135-19-3
Purity:
Appearance: broken white shiny flakes or white powder

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CasNo： 135-19-3

Molecular Formula： C₁₀H₈O

Appearance： broken white shiny flakes or white powder

Manufacturer Supply Best Quality 2-Naphthol 135-19-3 with Efficient Transportation

Molecular Formula:C10H8O
Molecular Weight:144.173
Appearance/Colour:broken white shiny flakes or white powder
Vapor Pressure:0.00162mmHg at 25°C
Melting Point:120-122 °C(lit.)
Refractive Index:1.677
Boiling Point:285.499 °C at 760 mmHg
Flash Point:144.002 °C
PSA：20.23000
Density:1.182 g/cm³
LogP:2.54540

2-Naphthalenol(Cas 135-19-3) Usage

General Description

2-Naphthalenol is a white crystalline compound with a strong, sweet, floral odor. It is derived from naphthalene and is used as a fragrance ingredient in the production of perfumes, soaps, and other cosmetic products. It is also used as a chemical intermediate in the synthesis of other compounds, such as insecticides and pharmaceuticals. 2-Naphthalenol is not considered to be highly toxic, but it can cause irritation to the skin, eyes, and respiratory system upon exposure. It is important to handle and store this chemical with care to prevent any potential health and safety risks.

InChI:InChI=1/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H

135-19-3 Relevant articles

-

Maikopar

, (1869)

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, p. 244 - 254 (2015)

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, p. 609 - 626 (1997)

1. Following a 0.25-mg/kg intrapericardi...

-

Warren,Smiles

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, p. 72 - 75 (2016)

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, p. 2905 - 2908 (1984)

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-

Soffer et al.

, p. 1556 (1952)

-

Wessely,Grill

, p. 282,286 (1947)

Mechanistic Insights into Hydrogen Evolution by Photocatalytic Reforming of Naphthalene

Al-Madanat, Osama,Alsalka, Yamen,Bahnemann, Detlef W.,Curti, Mariano,Dillert, Ralf

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Prasomsri, Teerawit,Galiasso Tailleur, Roberto E.,Alvarez, Walter E.,Sooknoi, Tawan,Resasco, Daniel E.

, p. 140 - 146 (2010)

The conversion of pure 1-tetralone and i...

-

Linstead,Michaelis

, p. 1134,1138 (1940)

-

Hodgkinson,Limpach

, p. 1096 (1891)

Formation of naphthalene hydrates in the enzymatic conversion of 1,2-dihydronaphthalene by two fungal peroxygenases and subsequent naphthalene formation

Kluge, Martin,Ullrich, Rene,Scheibner, Katrin,Hofrichter, Martin

, p. 56 - 60 (2014)

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Miyake, Yoshikazu,Owari, Takuya,Ishiga, Fumio,Teramoto, Masaaki

, p. 979 - 986 (1994)

The catalytic hydrolysis rates of a hydr...

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, (2019)

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Olah, George A.,Keumi, Takashi,Lecoq, Jean Claud,Fung, Alexander P.,Olah, Judith A.

, p. 6148 - 6151 (1991)

The acid-catalyzed hydroxylation of naph...

Mechanistic imperatives for catalysis of aldol addition reactions: Partitioning of the enolate intermediate between reaction with bronsted acids and the carbonyl group

Richard, John P.,Nagorski

, p. 4763 - 4770 (1999)

The lyoxide ion catalyzed intramolecular...

Selective Reductive Cleavage of Arenocrown Ethers by Alkali Metals in THF

Sokol, Maria,Kowalczuk, Marek,Grobelny, Zbigniew,Janeczek, Henryk,Jedlinski, Zbigniew,et al.

, p. 2365 - 2367 (1995)

Alkali metal solutions in tetrahydrofura...

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, p. 2213 - 2214 (1984)

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Two channels of electron transfer observed for the reaction of n-butyl chloride parent radical cations with naphthols and hydroxybiphenyls

Mohan,Hermann,Naumov,Mittal,Brede

, p. 5754 - 5762 (1998)

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, p. 7238 - 7243 (2019)

Experiments show that 1,1′-bi-2-naphthol...

-

Klamann

, p. 814,819 (1953)

-

Kotlarek

, p. 67 (1973)

-

May

, p. 650 (1922)

Coordination of manganese porphyrins on amino-functionalized MCM-41 for heterogeneous catalysis of naphthalene hydroxylation

Yang, Fu,Gao, Shuying,Xiong, Cuirong,Wang, Haiqing,Chen, Jin,Kong, Yan

, p. 1035 - 1041 (2015)

The different amounts of [5,10,15,20-tet...

-

Land et al.

, p. 1885,1887 (1961)

Atropselective hydrolysis of chiral BiNoL-phosphate esters catalyzed by the phosphotriesterase from Sphingobium sp. TCM1

Xiang, Dao Feng,Narindoshvili, Tamari,Raushel, Frank M.

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Bacterial Oxidation of Naphtharene to 1-Naphthol

Inoue, Masami,Inoue, Tomoni,Okami, Mituaki,Sayama, Michio,Hirai, Yoshiro

, p. 1315 - 1316 (1994)

The oxidation of naphtharene in a liquid...

Effect of Confinement on the Properties of Sequestered Mixed Polar Solvents: Enzymatic Catalysis in Nonaqueous 1,4-Bis-2-ethylhexylsulfosuccinate Reverse Micelles

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, p. 1678 - 1685 (2016)

The influence of different glycerol, N,N...

-

Arzoumanidis,Rauch

, p. 4443,4444,4445 (1973)

-

Harrison

, p. 616 (1969)

Photocatalytic Reductive C-O Bond Cleavage of Alkyl Aryl Ethers by Using Carbazole Catalysts with Cesium Carbonate

Yabuta, Tatsushi,Hayashi, Masahiko,Matsubara, Ryosuke

, p. 2545 - 2555 (2021/02/01)

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Paragraph 0152-0159, (2021/05/29)

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

A general method for the demethylation, ...

Electrochemical phenothiazination of naphthylamines and its application in photocatalysis

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supporting information, p. 8512 - 8515 (2021/08/31)

N-Phenylphenothiazine as an inexpensive,...

135-19-3 Process route

: 4323-69-7
[1]naphthyl-nitro-amine

: 7732-18-5
water

: 91-20-3,71998-51-1,72931-45-4
naphthalene

: 134-32-7
1-amino-naphthalene

: 135-19-3
β-naphthol

Conditions

Conditions	Yield

: 13463-67-7
titanium dioxide

: 135-19-3
β-naphthol