56875-67-3 Usage
Description
METHYL CIS-7-HEXADECENOATE, 5% SOLUTION IN ETHANOL is a volatile compound derived from the bacteria Clostridium tetani, specifically known as (7Z)-7-Hexadecenoic acid methyl ester. It is a fatty acid ester that is soluble in ethanol and is used in various applications across different industries due to its unique properties.
Uses
Used in Pharmaceutical Industry:
METHYL CIS-7-HEXADECENOATE, 5% SOLUTION IN ETHANOL is used as a pharmaceutical agent for its potential antimicrobial and anti-inflammatory properties. METHYL CIS-7-HEXADECENOATE, 5% SOLUTION IN ETHANOL may be utilized in the development of new drugs targeting bacterial infections, particularly those caused by Clostridium tetani, the bacteria responsible for tetanus.
Used in Cosmetics Industry:
In the cosmetics industry, METHYL CIS-7-HEXADECENOATE, 5% SOLUTION IN ETHANOL is used as a fragrance ingredient and preservative. Its volatile nature allows it to provide a pleasant scent in various cosmetic products, while its antimicrobial properties help maintain product integrity and prevent contamination.
Used in Research and Development:
METHYL CIS-7-HEXADECENOATE, 5% SOLUTION IN ETHANOL is used as a research compound for studying the properties and potential applications of volatile fatty acid esters. This can include investigations into their antimicrobial, anti-inflammatory, and other biological activities, as well as their potential use in drug delivery systems and other therapeutic applications.
Used in Agricultural Industry:
In agriculture, METHYL CIS-7-HEXADECENOATE, 5% SOLUTION IN ETHANOL may be used as a natural pesticide or repellent due to its antimicrobial properties. It could be applied to crops to protect them from bacterial infections or used as a natural alternative to synthetic pesticides, reducing the environmental impact of agricultural practices.
Used in Environmental Science:
METHYL CIS-7-HEXADECENOATE, 5% SOLUTION IN ETHANOL can be employed in environmental science for its potential use in bioremediation and waste management. METHYL CIS-7-HEXADECENOATE, 5% SOLUTION IN ETHANOL's antimicrobial properties may help in the treatment of contaminated water or soil, promoting the growth of beneficial bacteria and reducing the presence of harmful pathogens.
Check Digit Verification of cas no
The CAS Registry Mumber 56875-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,7 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56875-67:
(7*5)+(6*6)+(5*8)+(4*7)+(3*5)+(2*6)+(1*7)=173
173 % 10 = 3
So 56875-67-3 is a valid CAS Registry Number.
56875-67-3Relevant articles and documents
Identification and synthesis of new sex-specific components of olive fruit fly (Bactrocera oleae) female rectal gland, through original Negishi reactions on supported catalysts
Fusini, Graziano,Barsanti, Davide,Angelici, Gaetano,Casotti, Gianluca,Canale, Angelo,Benelli, Giovanni,Lucchi, Andrea,Carpita, Adriano
, p. 4381 - 4389 (2018/07/21)
In the present study, eleven new sex-specific components extracted from female rectal gland of olive fruit flies were synthesized and identified. The quantitative determination of those components by GC and GC/EI-MS, at different moments of the insect life span, highlighted the growing trend of their secretion. While for the synthesis of saturated esters, conventional transesterification methods could be adopted, for the synthesis of unsaturated components, a Negishi cross-coupling between organozinc halides and (Z)-1-bromo-1-alkenes was developed. To the extent of our knowledge, this reaction represents the first example of supported-catalyst promoted Negishi coupling, between an alkylzinc reagent and an alkenyl halide.
Preapration of 7,8,16-trihydroxy-hexadecanoic acid from aleuritic acid and a synthesis of E/Z-7-hexadecen-1,16-olides and hexalure
Tewari, Neera,Rohatgi, Amit,Bhushan, Kumar Hari,Subramanian, G. B. V.
, p. 851 - 855 (2007/10/03)
Both threo/erythro 7,8,16-trihydroxy-hexadecanoic acids have been preapred from threo/erythro 9,10,16-trihydroxy-hexadecanoic acids (aleuritic acid), by interchanging the positions of the terminal carboxyl and hydroxyl groups through steps of appropriate oxidation-reduction on the dithianes obtained from the 16-oxo-9,10-dihydroxy-hexadecanoic acids.Cyclization of the corresponding 9,10-olefin with dibutyl tin oxide furnish E/Z-7-hexadecen-1,16-olides.Preparation of the insect pheromone hexalure is also reported.
