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[RUI (-) TETRAME-BITIOP (P-CYMENE)] is a chemical compound formed by the combination of RUI (-), an organic molecule with potential anti-cancer and anti-inflammatory properties, and TETRAME-BITIOP (P-CYMENE), a monoterpene compound with antimicrobial and antioxidant properties. [RUI (-) TETRAME-BITIOP (P-CYMENE)] may exhibit synergistic effects and has potential applications in various fields, including medicine, agriculture, and industry.

266316-93-2

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266316-93-2 Usage

Uses

Used in Pharmaceutical Industry:
[RUI (-) TETRAME-BITIOP (P-CYMENE)] is used as a potential therapeutic agent for its anti-cancer and anti-inflammatory properties. [RUI (-) TETRAME-BITIOP (P-CYMENE)] may help in the development of new drugs to treat various types of cancer and inflammatory conditions.
Used in Agricultural Industry:
[RUI (-) TETRAME-BITIOP (P-CYMENE)] is used as a natural antimicrobial agent to protect crops from diseases and pests. Its antioxidant properties may also help in preserving the freshness and quality of agricultural products.
Used in Industrial Applications:
[RUI (-) TETRAME-BITIOP (P-CYMENE)] can be utilized in the development of new materials with enhanced antimicrobial and antioxidant properties, such as coatings, paints, and packaging materials, to improve their durability and safety.

Check Digit Verification of cas no

The CAS Registry Mumber 266316-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,6,3,1 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 266316-93:
(8*2)+(7*6)+(6*6)+(5*3)+(4*1)+(3*6)+(2*9)+(1*3)=152
152 % 10 = 2
So 266316-93-2 is a valid CAS Registry Number.

266316-93-2Downstream Products

266316-93-2Relevant academic research and scientific papers

Process-scale total synthesis of nature-identical (-)-(S,S)-7- hydroxycalamenal in high enantiomeric purity through catalytic enantioselective hydrogenation

Benincori, Tiziana,Bruno, Silvana,Celentano, Giuseppe,Pilati, Tullio,Ponti, Alessandro,Rizzo, Simona,Sada, Mara,Sannicolo, Francesco

, p. 1776 - 1789 (2007/10/03)

A process-scale stereoselective synthesis of nature-identical (-)-(S,S)-7-hydroxycalamenal (=(-)-(5S,85)-5,6,7,8-tetrahydro-3-hydroxy-5- methyl-8-(1-methylethyl)naphthalene-2-carbaldehyde; (-)-1α) in 96% enantiomeric excess (ee) with the aid of chiral Ru

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