66644-68-6 Usage
Description
ETHYL 3-METHYLBENZOYLFORMATE, also known as ethyl 3-methylbenzoylformate, is a colorless to pale yellow liquid chemical compound with the molecular formula C11H12O3. It possesses a fruity odor and is commonly utilized as a flavoring agent in the food and beverage industry. Additionally, it finds applications in the synthesis of other organic compounds and as a fragrance in cosmetic and personal care products. With its low toxicity and general safety for use in food and consumer products when following good manufacturing practices, it is a valuable component in various industries.
Uses
Used in Food and Beverage Industry:
ETHYL 3-METHYLBENZOYLFORMATE is used as a flavoring agent for its fruity odor, enhancing the taste and aroma of various food and drink products.
Used in Cosmetic and Personal Care Products:
ETHYL 3-METHYLBENZOYLFORMATE is used as a fragrance component in cosmetic and personal care products, providing a pleasant scent and improving the sensory experience for users.
Used in Organic Synthesis:
ETHYL 3-METHYLBENZOYLFORMATE is used as a key intermediate in the synthesis of other organic compounds, contributing to the development of new chemical products and materials.
It is important to handle and store ETHYL 3-METHYLBENZOYLFORMATE carefully to avoid exposure and potential hazards, ensuring the safety and quality of the final products in which it is used.
Check Digit Verification of cas no
The CAS Registry Mumber 66644-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,4 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66644-68:
(7*6)+(6*6)+(5*6)+(4*4)+(3*4)+(2*6)+(1*8)=156
156 % 10 = 6
So 66644-68-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O3/c1-3-14-11(13)10(12)9-6-4-5-8(2)7-9/h4-7H,3H2,1-2H3
66644-68-6Relevant articles and documents
Electrochemical two-electron oxygen reduction reaction (ORR) induced aerobic oxidation of α-diazoesters
Chen, Liang,Gao, Meng,Lu, Cuifen,Ma, Chao,Ruan, Mengyao,Wen, Ziyang,Yang, Fan,Yang, Guichun
, p. 2168 - 2171 (2022/02/17)
Electrochemical oxygen reduction reaction (ORR) is a powerful tool for introducing oxygen functional groups in synthetic chemistry. However, compared with the well-developed one-electron oxygen reduction process, the applications of two-electron oxygen re
Controllable chemoselectivity in the coupling of bromoalkynes with alcohols under visible-light irradiation without additives: Synthesis of propargyl alcohols and α-ketoesters
Ni, Ke,Meng, Ling-Guo,Ruan, Hongjie,Wang, Lei
supporting information, p. 8438 - 8441 (2019/07/22)
The chemoselectivity of visible-light-induced coupling reactions of bromoalkynes with alcohols can be controlled by simple changes to the reaction atmosphere (N2 or O2). A N2 atmosphere favours propargyl alcohols via a direct C-C coupling process, whereas an O2 atmosphere results in the generation of α-ketoesters through the oxidative CC/C-O coupling pathway.
COMPOUNDS HAVING MUSCARINIC RECEPTOR ANTAGONIST AND BETA2 ADRENERGIC RECEPTOR AGONIST ACTIVITY
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Paragraph 0398, (2016/09/12)
Compounds of formula I, defined herein, act both as muscarinic receptor antagonists and beta2 adrenergic receptor agonists and are useful for treating broncho-obstructive and inflammatory diseases.
