960149-22-8 Usage
Structure
Cyclooctyne ring with two fluorine atoms attached and an acetic acid functional group The compound has a unique structure that includes a cyclooctyne ring (eight-carbon ring with a triple bond) and two fluorine atoms, as well as an acetic acid group (carboxylic acid).
Synthetic compound
2-((6,6-difluorocyclooct-4-yn-1-yl)oxy)acetic acid is a man-made chemical and not found naturally occurring.
Potential applications
Organic synthesis and chemical research Due to its unique structure and reactivity, 2-((6,6-difluorocyclooct-4-yn-1-yl)oxy)acetic acid may be used in various organic chemistry reactions or as a building block for more complex compounds.
Reagent and building block
The compound may serve as a reagent in organic chemistry reactions or as a building block for synthesizing other complex compounds.
Further research and testing needed
The specific properties and potential uses of 2-((6,6-difluorocyclooct-4-yn-1-yl)oxy)acetic acid are yet to be determined and require additional research and testing.
Check Digit Verification of cas no
The CAS Registry Mumber 960149-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,1,4 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 960149-22:
(8*9)+(7*6)+(6*0)+(5*1)+(4*4)+(3*9)+(2*2)+(1*2)=168
168 % 10 = 8
So 960149-22-8 is a valid CAS Registry Number.
960149-22-8Relevant academic research and scientific papers
Compositions and methods for modification of biomolecules
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, (2016/03/12)
The present invention provides modified cycloalkyne compounds; and method of use of such compounds in modifying biomolecules. The present invention features a cycloaddition reaction that can be carried out under physiological conditions. In general, the invention involves reacting a modified cycloalkyne with an azide moiety on a target biomolecule, generating a covalently modified biomolecule. The selectivity of the reaction and its compatibility with aqueous environments provide for its application in vivo (e.g., on the cell surface or intracellularly) and in vitro (e.g., synthesis of peptides and other polymers, production of modified (e.g., labeled) amino acids).
