116920-31-1 Usage
Explanation
Different sources of media describe the Explanation of 116920-31-1 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Fontelis is the commercial name used for 1,3-Benzenediol, 2-chloro-4,6-dinitro-.
3. It is a man-made chemical used to control pests, specifically fungi, in agriculture.
4. The main application of this compound is to control fungal diseases in crops.
5. The compound works by blocking the succinate dehydrogenase enzyme, which is essential for energy production in fungi, thus disrupting their growth.
6. 1,3-Benzenediol, 2-chloro-4,6-dinitroposes significant health risks due to its high toxicity.
7. Due to its toxicity and potential carcinogenic effects, the use of 1,3-Benzenediol, 2-chloro-4,6-dinitrois controlled to ensure human and environmental safety.
Type of chemical compound
Synthetic pesticide
Primary use
Fungicide
Target crops
Apples, grapes, and tomatoes
Mechanism of action
Inhibition of succinate dehydrogenase enzyme
Toxicity
Highly toxic
Carcinogenic potential
Potentially carcinogenic
Regulatory status
Strictly regulated
Check Digit Verification of cas no
The CAS Registry Mumber 116920-31-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,9,2 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 116920-31:
(8*1)+(7*1)+(6*6)+(5*9)+(4*2)+(3*0)+(2*3)+(1*1)=111
111 % 10 = 1
So 116920-31-1 is a valid CAS Registry Number.
116920-31-1Relevant articles and documents
Micellar catalyzed hydroxylation of 1,2,3-trichloro-4,6-dinitrobenzene: Role of cationic head group–π interaction
Ravani, Ankita,Shukla, Atindra,Sastry, Nandhibatla Vishwanada,Shah, Dinesh Ochhavlal,Mishra, Manish Kumar
, (2020/01/28)
The micellar catalysis of the hydroxylation of 1,2,3-trichloro-4,6-dinitrobenzene (DNTCB) with aqueous NaOH, to synthesize 2-chloro-4,6-dinitroresorcinol (CDNR), was studied using cationic, anionic and non-ionic surfactants at different concentrations to
Synthesis of diaminoresorcinal from resorcinol
-
, (2008/06/13)
The invention relates to a novel process for preparing 4,6-diaminoresorcinol, a precursor to polybenzoxazole, from resorcinol according to the following scheme. STR1 Resorcinol (I) is reacted with a di-tert-alkylating reagent to form a 4,6,-di-tert-alkylresorcinol (II), which is then halogenated to form a 2-halo-4,6-di-tert-alkylresorcinol (III). The 2-halo-4,6-di-tert-alkylresorcinol is nitrated in one of two ways to form a 2-halo-4,6-dinitroresorcinol (IV), which is then hydrogenated to from the 4,6-diaminoresorcinol. The invention also relates to a novel chemical composition-2-halo-4,6-di-tert-alkylresorcinol (III )--and a process for preparing same.
