61468-39-1 Usage
Uses
Used in Chemical Synthesis:
1-tert-Butyl-3-chloro-5-methylbenzene is used as an intermediate in the chemical synthesis of various organic compounds. Its unique structure and reactivity make it a valuable component in the production of a range of chemical products.
Used in Solvent Applications:
1-tert-Butyl-3-chloro-5-methylbenzene is utilized as a solvent in various industrial processes. Its ability to dissolve a wide range of substances makes it a versatile option for different applications within the chemical industry.
Used in Polymer Production:
1-tert-Butyl-3-chloro-5-methylbenzene is also employed in the production of polymers. Its chemical properties contribute to the formation of polymers with specific characteristics, which are then used in a variety of end products.
Used in Industrial Applications:
Beyond its role in chemical synthesis, solvent applications, and polymer production, 1-tert-Butyl-3-chloro-5-methylbenzene finds use in other industrial applications. Its versatility and chemical properties make it suitable for a range of processes and products within the industry.
It is crucial to adhere to proper safety measures and handling procedures when working with 1-tert-Butyl-3-chloro-5-methylbenzene, as it can pose health risks if it comes into contact with the skin or is inhaled.
Check Digit Verification of cas no
The CAS Registry Mumber 61468-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,6 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61468-39:
(7*6)+(6*1)+(5*4)+(4*6)+(3*8)+(2*3)+(1*9)=131
131 % 10 = 1
So 61468-39-1 is a valid CAS Registry Number.
61468-39-1Relevant academic research and scientific papers
3,3-diphenyl prop-2-yl amino acid derivatives and their use as tachykinin antagonists
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, (2008/06/13)
Compounds of formula (I), or a salt or prodrug thereof, wherein R1 represents H, C1-4 alkyl or CH2 COOH; R2 represents H or C1-4 alkyl, with the proviso that R1 and R2 are not both H; R3 and R4 each independently rely resent H, C1-, alkyl. C2-6 alkenyl C1-6 alkoxy, halo or trifluoromethyl; A1, A2, A3, and A4 each independently represent H, C1-6 alkyl, C1-6 alkenyl, C1-6 alkoxy, halo or trifluoromethyl; and A5 and A6 each independently represent H or C1-4 are tachykinin antagonists useful STR1
