3354-56-1 Usage
Description
Phenol, 2-(1-methylethyl)-6-(2-propenyl)-, also known as 2-Allyl-6-isopropylphenol, is an organic compound with a phenolic structure. It is characterized by the presence of a hydroxyl group attached to a benzene ring, with an isopropyl and an allyl group as substituents. Phenol, 2-(1-methylethyl)-6-(2-propenyl)is known for its chemical reactivity and is commonly used as a building block in the synthesis of various pharmaceutical compounds.
Uses
Used in Pharmaceutical Industry:
Phenol, 2-(1-methylethyl)-6-(2-propenyl)is used as an intermediate in the synthesis of Propofol (P829750) and related compounds. Propofol is a widely used anesthetic agent in the medical field, known for its rapid onset and short duration of action. Phenol, 2-(1-methylethyl)-6-(2-propenyl)-'s role as an intermediate in the production of Propofol highlights its importance in the development of essential pharmaceuticals.
Phenol, 2-(1-methylethyl)-6-(2-propenyl)is also used as a precursor in the synthesis of various derivatives, which can have potential applications in different industries, such as the chemical, material science, and pharmaceutical sectors. These derivatives can be utilized in the development of new drugs, advanced materials, or other specialized products, further expanding the compound's utility and relevance in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 3354-56-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3354-56:
(6*3)+(5*3)+(4*5)+(3*4)+(2*5)+(1*6)=81
81 % 10 = 1
So 3354-56-1 is a valid CAS Registry Number.
3354-56-1Relevant articles and documents
GABAA Receptor allosteric enhancement compounds and their preparation and use
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Paragraph 0085-0086; 0090-0091, (2020/03/17)
A GABA A receptor allosteric enhancer compound and preparation and a use thereof are disclosed. The compound has a structure represented by formula (1). R 1 and R 2 are each independently selected from isopropyl and n-propyl; and when R 1 is n-propyl, R 2 is not isopropyl.
Water-Accelerated Claisen Rearrangements
Wipf, Peter,Rodriguez, Sonia
, p. 434 - 440 (2007/10/03)
Allyl aryl ethers undergo accelerated Claisen and [1,3] rearrangements in the presence of a mixture of trialkylalanes and water or aluminoxanes. The ratio of ortho-, meta-, and pora-Claisen products depends to a large extent on the presence of water and to a much lesser extent on the nature of the alane.
