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2,3,5,6-Tetramethyl-1,4-benzenediacetonitrile is a chemical compound with the molecular formula C12H16N2. It is a derivative of benzenediacetonitrile, characterized by the presence of four methyl groups attached to the benzene ring. This structural feature endows it with unique properties, making it a valuable building block in the synthesis of complex organic molecules.

1675-71-4

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1675-71-4 Usage

Uses

Used in Organic Chemistry:
2,3,5,6-Tetramethyl-1,4-benzenediacetonitrile is used as a precursor for the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of complex molecules, making it a versatile component in organic synthesis.
Used in Pharmaceutical Industry:
2,3,5,6-Tetramethyl-1,4-benzenediacetonitrile is used as a building block for the development of new drugs. Its potential applications in this field are due to its ability to contribute to the formation of diverse molecular structures that may possess therapeutic properties.
Used in Dye and Pigment Synthesis:
2,3,5,6-Tetramethyl-1,4-benzenediacetonitrile is used as a precursor for the synthesis of dyes and pigments. Its chemical structure provides a foundation for the creation of specialty chemicals that are used in various industries, such as textiles and plastics, for coloration purposes.
Used in Specialty Chemicals Production:
2,3,5,6-Tetramethyl-1,4-benzenediacetonitrile is used as a starting material for the production of specialty chemicals. Its role in this industry is to provide a base for the synthesis of compounds that have specific applications, such as in the development of new materials or the improvement of existing ones. The precise uses and applications of 2,3,5,6-Tetramethyl-1,4-benzenediacetonitrile may vary depending on the specific industry and research needs.

Check Digit Verification of cas no

The CAS Registry Mumber 1675-71-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1675-71:
(6*1)+(5*6)+(4*7)+(3*5)+(2*7)+(1*1)=94
94 % 10 = 4
So 1675-71-4 is a valid CAS Registry Number.

1675-71-4SDS

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 2-[4-(cyanomethyl)-2,3,5,6-tetramethylphenyl]acetonitrile

1.2 Other means of identification

Product number -
Other names 1,4-Benzenediacetonitrile,2,3,5,6-tetramethyl

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:1675-71-4 SDS

1675-71-4Relevant academic research and scientific papers

Syntheses of -, -, and Paracyclophanes with 1,2,4,5-Tetracyanobenzene Units as Electron Acceptors

Staab, Heinz A.,Wahl, Peter,Kay, Kwang-Yol

, p. 541 - 550 (2007/10/02)

Paracyclophanes 1 - 4 containing tetracyanobenzene (TCNB) units opposite to different electron donor components have been synthesized via the corresponding substituted dithiaparacyclophanes 8, 10, 12, and 14.For the pyrolysis of the disulfones 9

OXIDATION OF HEXAMETHYLBENZENE AND 2,3,4,5,6-PENTAMETHYLBENZYL CATION IN FLUOROSULFONIC ACID

Rudenko, A. P.,Zarubin, M. Ya.,Fedorova, E. M.

, p. 1609 - 1618 (2007/10/02)

The oxidation of hexamethylbenzene in HSO3F-PbO2 takes place with the participation of the 1-H+-1,2,3,4,5,6-hexamethylbenzenonium ion and the intermediate formation of the 2,3,4,5,6-pentamethylbenzyl cation, which is capable of entering into further oxidative transformations leading to substitution of the hydrogen atom in two and three methyl groups.The structure of the final products from the observed transformations were established, and a mechanism is proposed for their formation.

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