382162-24-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This is an alternative name for the compound, which is derived from its structure and functional groups.
Explanation
The compound is a derivative of catechol, which is a type of phenol, a class of organic compounds containing a hydroxyl group (-OH) bonded directly to an aromatic hydrocarbon.
Explanation
The structure describes the arrangement of atoms and functional groups in the compound, with two hydroxyl groups (-OH) at the 1 and 2 positions of the benzene ring, and two chloromethyl groups (-CH2Cl) at the 3 and 6 positions.
Explanation
The compound is used in various industrial applications, including the production of polymers and resins, as well as in the synthesis of pharmaceuticals and agrochemicals.
Explanation
The compound is toxic and can cause harm to human health and the environment if not properly managed. This highlights the importance of handling and disposing of the compound with care.
Explanation
Due to its toxicity, it is crucial to handle 1,2-Benzenediol, 3,6-bis(chloromethyl)(9CI) with care to minimize the risk of exposure and potential harm to humans and the environment.
Type
Phenol derivative
Structure
1,2-Benzenediol, 3,6-bis(chloromethyl)-
Applications
Production of polymers and resins, synthesis of pharmaceuticals and agrochemicals
Toxicity
Toxic to human health and the environment
Precaution
Handle with care
Check Digit Verification of cas no
The CAS Registry Mumber 382162-24-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,2,1,6 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 382162-24:
(8*3)+(7*8)+(6*2)+(5*1)+(4*6)+(3*2)+(2*2)+(1*4)=135
135 % 10 = 5
So 382162-24-5 is a valid CAS Registry Number.
382162-24-5Relevant academic research and scientific papers
Electroorganic reactions. Part 55. Quinodimethane chemistry. Part 3. Transition metal complexes as inter- and intra-molecular redox catalysts for the electrosynthesis of poly(p-xylylene) (PPX) polymers and oligomers
Janssen,Utley,Carre?,Simon,Schirmer
, p. 1573 - 1584 (2007/10/03)
The role of metal complexes as redox mediators in the electrosynthesis of poly(p-xylylenes) (PPXs) has been explored, with a view to designing metal-containing precursors that can act both as mediators and starting materials for metal-containing polymers. A number of transition metal complexes [Cr(III), Ni(II) and Co(II)] are efficient redox catalysts for production of quinodimethanes, and hence PPXs. Following encouraging results from experiments using mediators based on anthranilic acid and salicylaldehyde ligands a macrocyclic compound was designed, and successfully prepared by a convergent route that incorporated both a 1,4-bis(chloromethylarene) function as a precursor to a quinodimethane and a Ni(II) salen unit as an intramolecular redox catalyst. The macrocycle was successfully reduced cathodically to yield a PPX polymer with bound Ni(II). Evidence is presented for the operation of intramolecular redox catalysis (homomediation).
