5077-75-8 Usage
Description
2,6-Dichlorocapronic acid, also known as 2,6-Dichlorohexanoic acid, is a chemical compound with the formula C6H10Cl2O2. It is a derivative of caproic acid, featuring chlorine atoms attached to the 2nd and 6th carbon positions. This white crystalline solid at room temperature possesses a strong, unpleasant odor and is known for its corrosive and irritating properties, necessitating careful handling and storage in a ventilated area with appropriate protective equipment to prevent exposure.
Uses
Used in Pharmaceutical Production:
2,6-Dichlorocapronic acid is used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of drugs with specific therapeutic properties.
Used in Pesticide Manufacturing:
In the agricultural sector, 2,6-Dichlorocapronic acid serves as a precursor in the production of certain pesticides. Its chemical properties contribute to the effectiveness of these products in controlling pests and ensuring crop protection.
Used in Organic Chemical Synthesis:
Beyond its applications in pharmaceuticals and pesticides, 2,6-Dichlorocapronic acid is also utilized in the synthesis of other organic chemicals. Its versatility in chemical reactions makes it a valuable compound in the creation of a wide range of specialty chemicals for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5077-75-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,7 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5077-75:
(6*5)+(5*0)+(4*7)+(3*7)+(2*7)+(1*5)=98
98 % 10 = 8
So 5077-75-8 is a valid CAS Registry Number.
5077-75-8Relevant articles and documents
Decyclization of chlorocyclohexanone hydroperoxides under the action of ferrous salts
Starostin,Gushchin,Ignatenko,Aleksandrov,Nikishin
, p. 133 - 136 (2007/10/03)
The decomposition of 2-chloro-, 2,2-dichloro-, and 2,6-dichloro-substituted cyclohexanone hydroperoxides on treatment with ferrous chloride and sulfate to give chloro-substituted aliphatic acids was investigated. A method for the synthesis of 2,6,6-trichlorohexanoic and 2,6,7,11-tetrachlorododecane-1,12-dioic acids was elaborated.
