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136911-16-5

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136911-16-5 Usage

General Description

Benzenemethanol, 3-methoxy-2-(2-propenyl)-, also known as eugenol, is a naturally occurring compound found in cloves, nutmeg, and cinnamon. It is a colorless to pale yellow liquid with a strong, spicy odor and taste. Eugenol is commonly used as a flavoring agent in food and beverages, as well as in the fragrance and pharmaceutical industries. It also possesses antimicrobial, antioxidant, and analgesic properties, making it a valuable compound in traditional medicine and natural health products. Additionally, eugenol has been studied for its potential anti-inflammatory and anti-cancer effects, showing promising results in preliminary research.

Check Digit Verification of cas no

The CAS Registry Mumber 136911-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,9,1 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136911-16:
(8*1)+(7*3)+(6*6)+(5*9)+(4*1)+(3*1)+(2*1)+(1*6)=125
125 % 10 = 5
So 136911-16-5 is a valid CAS Registry Number.

136911-16-5Relevant articles and documents

AMINE SALTS OF A PROSTACYCLIN ANALOG

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Paragraph 0339; 0340, (2015/06/03)

The present invention provides amine salts of the prostacyclin analogue of Formula I and processes for generating these amine salts.

1-(PIPERIDIN-4-YL)-1H-INDOLE DERIVATIVE

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Page/Page column 83, (2010/11/28)

The present invention provides a compound represented by the formula (1) or a pharmacologically acceptable salt thereof, or a hydrate thereof (provided that a compound in which all of R4a, R4b, and R4c are hydrogen atoms is excluded.): [wherein R1 represents a hydrogen atom, R2 represents a hydrogen atom, R3 represents the formula: wherein R4a, R4b, and R4c are the same as or different from each other and each represents a hydrogen atom, a C1-6 alkyl group or a C1-6 alkoxy group, etc.]

Palladium-catalyzed carbonylative cyclization via trapping of acylpalladium derivatives with internal enolates. Its scope and factors affecting the C-to-O ratio

Negishi, El-Ichi,Coperet, Christophe,Sugihara, Takumichi,Shimoyama, Izumi,Zhang, Yantao,Wu, Guangzhong,Tour, James M.

, p. 425 - 436 (2007/10/02)

The Pd-catalyzed carbonylative cyclization reaction involving ω-acyl-substituted acylpalladium derivatives can proceed via intramolecular trapping with either C- or O-enolates; the preferential formation of either 5- or 6-membered rings dictates the C-to-

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