1161004-57-4 Usage
Uses
Used in Flavor and Fragrance Industry:
Ethyl 5,5-difluoro-4-oxopentanoate is used as a flavoring agent for its fruity odor, enhancing the sensory experience of various food products and beverages.
Used in Pharmaceutical Synthesis:
Ethyl 5,5-difluoro-4-oxopentanoate is used as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs due to its reactivity and the unique properties imparted by the fluorine atoms.
Used in Agrochemical Production:
In the agrochemical industry, Ethyl 5,5-difluoro-4-oxopentanoate is used as a precursor in the production of various agrochemicals, leveraging its versatility to create effective compounds for agricultural applications.
Used in Organic Chemistry Research:
Ethyl 5,5-difluoro-4-oxopentanoate is utilized as a building block in organic chemistry, facilitating the exploration of new reactions and the creation of novel organic compounds for a range of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1161004-57-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,1,0,0 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1161004-57:
(9*1)+(8*1)+(7*6)+(6*1)+(5*0)+(4*0)+(3*4)+(2*5)+(1*7)=94
94 % 10 = 4
So 1161004-57-4 is a valid CAS Registry Number.
1161004-57-4Relevant academic research and scientific papers
SUBSTITUTED OXOPYRIDINE DERIVATIVES
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Page/Page column 72-73, (2020/07/14)
The invention relates to substituted oxopyridine derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular vascular disorders, preferably thrombotic
SUBSTITUTED OXOPYRIDINE DERIVATIVES
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Page/Page column 60, (2020/07/14)
The invention relates to substituted oxopyridine derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular vascular disorders, preferably thrombotic
Concise synthesis of ω-fluoroalkylated ketoesters. A building block for the synthesis of six-, seven-, and eight-membered fluoroalkyl substituted 1,2-diaza-3-one heterocycles
Wan, Wen,Hou, Jie,Jiang, Haizhen,Wang, Yangli,Zhu, Shizheng,Deng, Hongmei,Hao, Jian
experimental part, p. 4212 - 4219 (2009/09/30)
A concise and general synthetic route toward the small and medium-sized fluoroalkyl substituted 1,2-diaza-3-one heterocyclic ring skeletons via a sequential reaction of condensation and ring-closure reaction of ω-fluoroalkylated ketoesters 4 with hydrazin
