130776-67-9 Usage
Uses
Used in Biological Studies:
2,2-DIMETHYLCAPRYLIC ACID is used as a metabolite in biological studies for understanding the metabolic pathways and ecological roles of sewage bacteria. As a benzyl dimethyloctanoate metabolite, it provides insights into the biotransformation processes and the ability of these bacteria to break down complex organic compounds in wastewater treatment systems.
Used in Environmental Applications:
2,2-DIMETHYLCAPRYLIC ACID is used as a biomarker for assessing the efficiency of wastewater treatment processes. Its presence in treated water can indicate the effectiveness of the treatment in breaking down and removing organic pollutants, thus contributing to the overall environmental health and safety.
Used in Chemical Research:
2,2-DIMETHYLCAPRYLIC ACID serves as a valuable compound in chemical research, particularly in the synthesis of various organic molecules and the development of new materials. Its unique structure makes it a potential candidate for the creation of novel chemical entities with specific properties and applications.
Used in Pharmaceutical Applications:
Although not explicitly mentioned in the provided materials, 2,2-DIMETHYLCAPRYLIC ACID could potentially be used in the pharmaceutical industry as a starting material for the synthesis of drugs or as an active ingredient itself, depending on its biological activity and pharmacological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 130776-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,7,7 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 130776-67:
(8*1)+(7*3)+(6*0)+(5*7)+(4*7)+(3*6)+(2*6)+(1*7)=129
129 % 10 = 9
So 130776-67-9 is a valid CAS Registry Number.
130776-67-9Relevant academic research and scientific papers
Copper-catalyzed cross-coupling of functionalized alkyl halides and tosylates with secondary and tertiary alkyl Grignard reagents
Ren, Peng,Stern, Lucas-Alexandre,Hu, Xile
supporting information, p. 9110 - 9113 (2012/10/29)
Added value: A copper-based method is highly efficient for the cross-coupling of alkyl electrophiles with secondary and tertiary alkyl Grignard reagents. The method is distinguished by its broad substrate scope and high functional group tolerance. Copyright
7-oxabicycloheptyl substituted heterocyclic amide or ester prostaglandin analogs useful in the treatment of thrombotic and vasospastic disease
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, (2008/06/13)
7-Oxabicycloheptane substituted prostaglandin analogs useful in treating thrombotic and vasopastic disease have the structural formula STR1 wherein m is 1, 2 or 3; n is 1, 2, 3 or 4; Z is --(CH2)2 --, --CH=CH-- or STR2 wherein Y is O, a single bond or vinyl, with the proviso that when n is 0, if Z is STR3 then Y cannot be O, and Z is --CH=CH--, n is 1, 2, 3 or 4; and when Y=vinyl, n=0; R is CO2 H, CO2 lower alkyl, CH2 OH, CO2 alkali metal, CONHSOR3, CONHR3a or --CH2 --5-tetrazolyl, X is O, S or NH; and where R1, R2, R3 and R3a are as defined herein.
Process for preparing silver catalysts
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, (2008/06/13)
A silver salt solution suitable for depositing silver on a support in the preparation of silver cata-lysts is made by reacting a silver compound with a neo-acid, in a hydrocarbon solvent. The reaction is completed under reflux conditions, thereby removing water formed by the rection and reacting at least 90% of the unreacted acid. The solution may be used without further processing to impregnate a porous support, thereby providing a catalyst useful for oxida-tion of ethylene oxide.
