What is the 1,4-Dimethylnaphthalene?

1,4-Dimethylnaphthalene is , while it's Molecular Formula is C12H12. Used in Chemical Production: 1,4-Dimethylnaphthalene is used as a synthetic intermediate for the production of various chemicals, leveraging its chemical structure to facilitate the synthesis of a range of compounds. Used in Dye and Pigment Industries: 1,4-Dimethylnaphthalene is utilized as a key component in the manufacturing of dyes and pigments, contributing to their color and stability. Used in Electronics and Semiconductor Industries: In the electronics and semiconductor sectors, 1,4-Dimethylnaphthalene is employed in processes that require its specific chemical properties, such as in the development of certain materials and components. Given the potential hazards associated with 1,4-Dimethylnaphthalene, it is crucial that its applications are carefully managed to mitigate any risks to health and the environment.

What is the CAS number for 1,4-Dimethylnaphthalene?

The CAS number of 1,4-Dimethylnaphthalene is 571-58-4.

What is 1,4-Dimethylnaphthalene (571-58-4) used for?

1,4-Dimethylnaphthalene, also known as 1,4-naphthalenedimethyl, is a chemical compound that belongs to the class of polycyclic aromatic hydrocarbons. It features a naphthalene ring with two methyl groups attached at the 1 and 4 positions, giving it a colorless to light yellow liquid appearance with a faint aromatic odor. Due to its chemical properties, it is considered a hazardous substance with potential health and environmental risks, necessitating proper handling and disposal.InChI:InChI=1/C12H12/c1-9-7-8-10(2)12-6-4-3-5-11(9)12/h3-8H,1-2H3

What is the 1,4-Dimethylnaphthalene?

1,4-Dimethylnaphthalene is , while it's Molecular Formula is C12H12. Used in Chemical Production: 1,4-Dimethylnaphthalene is used as a synthetic intermediate for the production of various chemicals, leveraging its chemical structure to facilitate the synthesis of a range of compounds. Used in Dye and Pigment Industries: 1,4-Dimethylnaphthalene is utilized as a key component in the manufacturing of dyes and pigments, contributing to their color and stability. Used in Electronics and Semiconductor Industries: In the electronics and semiconductor sectors, 1,4-Dimethylnaphthalene is employed in processes that require its specific chemical properties, such as in the development of certain materials and components. Given the potential hazards associated with 1,4-Dimethylnaphthalene, it is crucial that its applications are carefully managed to mitigate any risks to health and the environment.

What is the CAS number for 1,4-Dimethylnaphthalene?

The CAS number of 1,4-Dimethylnaphthalene is 571-58-4.

What is 1,4-Dimethylnaphthalene (571-58-4) used for?

1,4-Dimethylnaphthalene, also known as 1,4-naphthalenedimethyl, is a chemical compound that belongs to the class of polycyclic aromatic hydrocarbons. It features a naphthalene ring with two methyl groups attached at the 1 and 4 positions, giving it a colorless to light yellow liquid appearance with a faint aromatic odor. Due to its chemical properties, it is considered a hazardous substance with potential health and environmental risks, necessitating proper handling and disposal.InChI:InChI=1/C12H12/c1-9-7-8-10(2)12-6-4-3-5-11(9)12/h3-8H,1-2H3

Product classification

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571-58-4

Product Name:1,4-Dimethylnaphthalene
Molecular Formula:C12H12
Molecular Weight:156.227

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Product Details

pd_meltingpoint:−18 °C(lit.)

Purity:99%

Factory Sells Best Quality 1,4-Dimethylnaphthalene 571-58-4 with ISO standards

Molecular Formula:C12H12
Molecular Weight:156.227
Vapor Pressure:0.013mmHg at 25°C
Melting Point:−18 °C(lit.)
Boiling Point:268°Cat760mmHg
Flash Point:109.2°C
PSA：0.00000
Density:1g/cm³
LogP:3.45660

1,4-Dimethylnaphthalene(Cas 571-58-4) Usage

General Description

1,4-Dimethylnaphthalene, also known as 1,4-naphthalenedimethyl, is a chemical compound belonging to the class of polycyclic aromatic hydrocarbons. It is composed of a naphthalene ring with two methyl groups attached at the 1 and 4 positions. This chemical is commonly used in the production of dyes, pigments, and as a synthetic intermediate in the manufacturing of other chemicals. It also has applications in the electronics and semiconductor industries. 1,4-Dimethylnaphthalene is a colorless to light yellow liquid with a faint aromatic odor, and it is considered a hazardous substance with potential health and environmental risks if not handled and disposed of properly.

InChI:InChI=1/C12H12/c1-9-7-8-10(2)12-6-4-3-5-11(9)12/h3-8H,1-2H3

571-58-4 Relevant articles

Competition between Birch Reduction and Bond Cleavage in 1,2-Bis(4-methyl-1-naphthyl)ethane

Marcinow, Zbigniew,Hull, C. Eugene,Rabideau, Peter W.

, p. 3602 - 3605 (1989)

The reaction of 1,2-bis(4-methyl-1-napht...

"off-on" switching of intracellular singlet oxygen release under biocompatible conditions

Ucar, Esma,Xi, Dongmei,Seven, Ozlem,Kaya, Cansu,Peng, Xiaojun,Sun, Wen,Akkaya, Engin U.

, p. 13808 - 13811 (2019)

Precise spatiotemporal control of single...

Chemiluminescence during decomposition of 1,4-dimethylnaphthalene endoperoxide on the silica gel and alumina surface

Kazakov,Mal'tsev,Maistrenko,Khursan,Ovchinnikov,Kazakov

, p. 205 - 210 (2007)

Decomposition of 1,4-dimethylnaphthalene...

Tetrahydronaphthalene-1,4-dione and its chromiumtricarbonyl complex

Garcia, Alvaro Enriquez,Kuendig, E. Peter,Lomberget, Thierry,Bragg, Ryan,Poulard, Cyril,Bernardinelli, Gerald

, p. 169 - 171 (2007)

The article gives a brief outline of the...

Reactions of Sodium Borohydride in Acidic Media; IX. Deoxygenation of 1,4-Epoxy-1,4-dihydronaphtalenes; A Convenient Naphthalene Synthesis

Gribble, Gordon W.,Kelly, William J.,Sibi, Mukund P.

, p. 143 - 145 (1982)

Formal total synthesis of (±)-occidol

Vera, William J.,Banerjee, Ajoy K.

, p. 3091 - 3094 (2006)

The conversion of tetralone 1 to methylk...

Laser flash-chemiluminescence study of O2(1Δ) photoeliminated from 1,4- dimethylnaphthalene endoperoxide

Chou, Pi-Tai,Frei, Heinz

, p. 3843 - 3854 (1987)

Deactivation of O2(1Δ) photoeliminated f...

Nonradiative deactivation of singlet oxygen (1O2) by cubane and its derivatives

Lancaster, Jeffrey R.,Marti, Angel A.,Lopez-Gejo, Juan,Jockusch, Steffen,O'Connor, Naphtali,Turro, Nicholas J.

, p. 5509 - 5512 (2008)

(Chemical Equation Presented) The bimole...

141. The Vitamin-B12-derived Co(III)-Complex 'Pyrocobester' as Photosensitizer and as Substrate in Reactions Involving 'Singlet Oxygen'

Kraeutler, Bernhard,Stepanek, Rene

, p. 1493 - 1512 (1983)

The vitamin-B12 derivative 'pyrocobester...

The Reactions of O2 (1Δg) with Anancomeric 1,3-Dithianes. The First Experimental Evidence in Support of a Hydroperoxy Sulfonium Ylide as a Precursor to Sulfoxide on the Sulfide Singlet Oxygen Reaction Surface

Toutchkine,Clennan

, p. 5620 - 5625 (1999)

The kinetic isotope effects for the form...

Deoxygenation of Arene 1,4-Endoxides with Low-Valent Metals

Hart, Harold,Nwokogu, Godson

, p. 1251 - 1255 (1981)

Low-valent forms of iron, tungsten, and ...

Methylation of 2-methylnaphthalene over metal-impregnated mesoporous MCM-41 for the synthesis of 2,6-triad dimethylnaphthalene isomers

Niftaliyeva, Aysel,Güle?, Fatih,Karaduman, Ali

, p. 2403 - 2416 (2020)

2,6-Dimethylnaphthalene (2,6-DMN) is one...

Synthesis method of 1,4-dimethylnaphthalene

-

Paragraph 0032-0048, (2021/06/23)

The invention discloses a synthesis meth...

Synthesis of Nanosized ZSM-5 Zeolites by Different Methods and Their Catalytic Performance in the Alkylation of Naphthalene

Wang, Yongchao,Kikhtyanin,Li, Cheng,Su, Xiaofang,Bai, Xuefeng,Wu, Wei

, p. 394 - 406 (2021/02/26)

Abstract: Three nanosized ZSM-5 zeolites...

Synthesis of renewable alkylated naphthalenes with benzaldehyde and angelica lactone

Cong, Yu,Li, Guangyi,Li, Ning,Wang, Aiqin,Wang, Ran,Wang, Xiaodong,Xu, Jilei,Zhang, Tao

supporting information, p. 5474 - 5480 (2021/08/16)

Herein, we report a new route for the sy...

Iron-Catalyzed Direct Julia-Type Olefination of Alcohols

Landge, Vinod G.,Babu, Reshma,Yadav, Vinita,Subaramanian, Murugan,Gupta, Virendrakumar,Balaraman, Ekambaram

, p. 9876 - 9886 (2020/09/03)

Herein, we report an iron-catalyzed, con...

571-58-4 Process route

: C₁₅H₁₅N₃O₂

: 571-58-4
1,4-dimethylnaphthalene

: 13274-43-6
4-methyl-1,2,4-triazoline-3,5-dione

Conditions

Conditions	Yield
With 2,3-Dimethyl-2-butene; 1,1-dichloroethane; In chloroform-d1; at 29 ℃; Kinetics;

: 67-71-0
dimethylsulfone

: 20240-61-3
cis/trans-4-methyl-1,2,3,4-tetrahydro-1-naphthol

: 571-58-4
1,4-dimethylnaphthalene

: 1333-74-0
hydrogen

Conditions

Conditions	Yield
With 1,10-Phenanthroline; potassium tert-butylate; iron(II) chloride; In toluene; at 120 ℃; for 24h; Inert atmosphere; Schlenk technique;	48%

571-58-4 Upstream products

6627-78-7
1-bromo-4-methylnaphthalene
4705-94-6
1,4-dimethyl-2-naphthol
6586-89-6
1,4-bis(chloromethyl)naphthalene
14108-88-4
1,2,3,4-tetrahydro-5,8-dimethylnaphthalene

571-58-4 Downstream products

131543-46-9
Glyoxal
78-98-8
2-oxopropanal
58791-49-4
1,4-bis(bromomethyl)naphthalene
476-73-3
1,2,3,4-benzenetetracaboxylic acid

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