2216-84-4 Usage
Uses
Used in Chemical Synthesis:
1,2,3,4,5,6-Cyclohexanehexacarboxylic acid serves as a precursor in the synthesis of various organic compounds, leveraging its reactive carboxylic acid groups for the formation of esters, amides, and other derivatives.
Used in Pharmaceutical Industry:
1,2,3,4,5,6-Cyclohexanehexacarboxylic acid is utilized as a building block in the development of pharmaceuticals, contributing to the creation of novel drug molecules with potential therapeutic applications.
Used in Corrosion Inhibition:
As a corrosion inhibitor, 1,2,3,4,5,6-Cyclohexanehexacarboxylic acid is employed to protect metal surfaces from degradation, particularly in industrial settings where equipment is exposed to corrosive environments.
Used as a Complexing Agent for Metal Ions:
1,2,3,4,5,6-Cyclohexanehexacarboxylic acid functions as a complexing agent, capable of binding to metal ions to form stable complexes. This property is valuable in various applications, including water treatment and metal recovery processes.
Used in the Production of Synthetic Resins:
1,2,3,4,5,6-Cyclohexanehexacarboxylic acid is incorporated into the manufacturing process of synthetic resins, enhancing their properties and performance in a range of applications, from coatings to plastics.
Check Digit Verification of cas no
The CAS Registry Mumber 2216-84-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2216-84:
(6*2)+(5*2)+(4*1)+(3*6)+(2*8)+(1*4)=64
64 % 10 = 4
So 2216-84-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O12/c13-7(14)1-2(8(15)16)4(10(19)20)6(12(23)24)5(11(21)22)3(1)9(17)18/h1-6H,(H,13,14)(H,15,16)(H,17,18)(H,19,20)(H,21,22)(H,23,24)
2216-84-4Relevant academic research and scientific papers
Optically active phenoxypropionic esters
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, (2008/06/13)
Optically active compounds of the formula I STR1 where R is C1 -C12 -alkyl or -perfluoroalkyl in which one or two non-adjacent CH2 or CF2 groups can also be replaced by --O-- and/or --CO-- and/or --CO--O-- and/or --CH=CH-- and/or --CH-halogen-- and/or --CHCN-- and/or --0--CO--CH-halogen-- and/or --O--CO--CHCN--, or is C1 -C12 -alkyl which can have a terminal chemically reactive group and in which a CH2 group can be replaced by --O--, A1 and A2 are each, independently of one another, 1,4-phenylene which is unsubstituted or substituted by one or two F and/or Cl and/or Br atoms and/or CH3 groups and/or CN groups and in which one or two CH groups can also be replaced by N, 1,4-cyclohexylene in which one or two non-adjacent CH2 groups can also be replaced by --O-- and/or --S--, 1,4-piperidinediyl, 1,4-bicyclo[2.2.2]octylene, 2,6-naphthalenediyl, decahydro-2,6-naphthalenediyl or 1,2,3,4-tetrahydro-2,6-naphthalenediyl, A3 is unsubstituted or substituted phenyl, Z is --CO--O--, --O--CO--, --CH2 CH2 --, --OCH2 --, --CH2 O--, --C C-- or a single bond and m is 0, 1, 2 or 3.
