1985-64-4 Usage
Uses
Used in Chemical Production:
Benzene, 2-(1,1-dimethylethyl)-1,3-dimethylis utilized as a key solvent in the production of chemicals, where its solvent properties aid in the synthesis and processing of various chemical compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, Benzene, 2-(1,1-dimethylethyl)-1,3-dimethyl- serves as a solvent for the manufacturing process of different medications, contributing to the efficiency of drug production and formulation.
Used in Coatings and Adhesives:
Benzene, 2-(1,1-dimethylethyl)-1,3-dimethylis employed as a solvent in the formulation of coatings and adhesives, enhancing their performance characteristics such as adhesion, drying time, and durability.
Used in Cleaning Agents:
This chemical compound is also used in the production of cleaning agents, where its solvent properties help in the effective removal of dirt, grease, and other contaminants.
Used in Dye Manufacturing:
Benzene, 2-(1,1-dimethylethyl)-1,3-dimethylis a raw material in the manufacture of dyes, playing a crucial role in the coloration process of various products.
Used in Rubber and Plastics Industry:
It is also utilized in the rubber and plastics industry as a raw material, contributing to the development of specific properties in the final products such as flexibility, durability, and resistance to environmental factors.
Check Digit Verification of cas no
The CAS Registry Mumber 1985-64-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1985-64:
(6*1)+(5*9)+(4*8)+(3*5)+(2*6)+(1*4)=114
114 % 10 = 4
So 1985-64-4 is a valid CAS Registry Number.
1985-64-4Relevant academic research and scientific papers
CYCLOPHANES WITH LARGE INTERNAL SUBSTITUENTS. THE SYNTHESIS AND CONFORMATIONAL BEHAVIOR OF 2,11-DITHIAMETACYCLOPHANES AND A METHACYCLOPHANE WITH tert-BUTYL SUBSTITUENTS.
Mitchell, Reginald H.,Weerawarna, Kumudini S.,Bushnell, Gordon W.
, p. 907 - 910 (2007/10/02)
The preparation, 1Hmr spectra and stereochemistry of 1E, 3E, 2F, 3F, and 2G are described.The stereochemistry of 3E is supported by an X-ray structure determination.
