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1012085-51-6

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1012085-51-6 Usage

Description

Naphthalene, 1,4-bis(4-methylphenyl)-, also known as α,α'-dimethyl-1,4-diphenylbenzene, is a chemical compound with the molecular formula C24H20. It is a derivative of naphthalene, featuring two 4-methylphenyl groups attached at the 1 and 4 positions of the naphthalene ring. This white to off-white crystalline solid possesses a strong aromatic odor and is recognized for its potential applications in various industries.

Uses

Used in Organic Synthesis:
Naphthalene, 1,4-bis(4-methylphenyl)is utilized as a building block in the synthesis of various organic compounds. Its unique structure allows for the creation of complex molecules that can be used in a wide range of applications.
Used in Dye Production:
In the dye industry, Naphthalene, 1,4-bis(4-methylphenyl)serves as a chemical intermediate. Its properties contribute to the development of dyes with specific characteristics, such as color intensity and stability.
Used in Pharmaceutical Industry:
Naphthalene, 1,4-bis(4-methylphenyl)is also employed as a chemical intermediate in the production of pharmaceuticals. Its involvement in the synthesis of certain drugs highlights its importance in the development of new medications.
Used in Other Industrial Products:
Beyond dyes and pharmaceuticals, Naphthalene, 1,4-bis(4-methylphenyl)finds use in the manufacturing of other industrial products. Its versatility as a chemical intermediate makes it valuable in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1012085-51-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,2,0,8 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1012085-51:
(9*1)+(8*0)+(7*1)+(6*2)+(5*0)+(4*8)+(3*5)+(2*5)+(1*1)=86
86 % 10 = 6
So 1012085-51-6 is a valid CAS Registry Number.

1012085-51-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis(4-methylphenyl)naphthalene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1012085-51-6 SDS

1012085-51-6Downstream Products

1012085-51-6Relevant articles and documents

Diels-alder reaction of isobenzofurans/cyclopentadienones with tetrathiafulvalene: Preparation of naphthalene, fluoranthene, and fluorenone derivatives

Karunakaran, Jayachandran,Mohanakrishnan, Arasambattu K.

supporting information, p. 966 - 970 (2018/02/23)

Diels-Alder reaction of 1,3-diarylbenzo[c]furan/cyclopentadienone with TTF followed by triflic acid mediated cleavage of the resulting adducts led to the formation of the respective 1,4-diaryl substituted naphthalenes, fluoranthenes, and fluorenones. The photophysical properties of representative diaryl-substituted hydrocarbons are also reported.

Cross-coupling of aryl/alkenyl ethers with aryl grignard reagents through nickel-catalyzed C-O activation

Xie, Lan-Gui,Wang, Zhong-Xia

supporting information; experimental part, p. 4972 - 4975 (2011/06/17)

The formation of a C-C bond has been achieved through the cleavage of the sp2 C-O bond of aryl/alkenyl ethers catalyzed by a nickel complex, and by using Grignard reagents as nucleophiles (see scheme). This method displays a broad substrate scope and leads to good to excellent yields of the aryl-aryl or alkenyl-aryl cross-coupling products.

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