22978-61-6 Usage
General Description
3,5-Dichlorobenzene-1-carboximidamide hydrochloride is a chemical compound that is commonly used as a fungicide and bactericide in agricultural and horticultural applications. It is a white crystalline solid that is soluble in water and organic solvents. 3,5-DICHLOROBENZENE-1-CARBOXIMIDAMIDE HYDROCHLORIDE is effective in controlling a wide range of fungal and bacterial diseases in crops and plants, making it a valuable tool for pest and disease management in agriculture. It works by inhibiting the growth and reproduction of harmful microorganisms, thereby protecting plants from infections and promoting healthier growth. Overall, 3,5-Dichlorobenzene-1-carboximidamide hydrochloride is an important chemical for maintaining the health and productivity of crops and plants in agricultural settings.
Check Digit Verification of cas no
The CAS Registry Mumber 22978-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,7 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22978-61:
(7*2)+(6*2)+(5*9)+(4*7)+(3*8)+(2*6)+(1*1)=136
136 % 10 = 6
So 22978-61-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Cl2N2.ClH/c8-5-1-4(7(10)11)2-6(9)3-5;/h1-3H,(H3,10,11);1H
22978-61-6Relevant articles and documents
Preparation of Triazolopyrimidines as Potential Antiasthma Agents
Medwid, Jeffrey B.,Paul, Rolf,Baker, Jannie S.,Brockman, John A.,Du, Mila T.,et al.
, p. 1230 - 1241 (2007/10/02)
With the use of the human basophil histamine release assay, 5-aryl-2-aminotriazolopyrimidines were found to be active as mediator release inhibitors.These compounds were prepared by reacting arylamidines with sodium ethyl formylacetate or with ethyl propiolate to give pyrimidinones.Treatment with phosphorus oxychloride gave a chloropyrimidine, which was converted to a hydrazinopyrimidine with hydrazine.Cyclization, using cyanogen bromide, gave the triazolopyrimidines, after a Dimroth rearrangement.Following a structure-activity evaluation, the5--2-amino (8-10), 5-(3-bromophenyl)-2-amino (8-13), 5--2-amino (8-11), and 5-(4-pyridinyl)-2-amino (6-7) compounds were found to have the best activity.They were chosen for further pharmacological and toxicological study.
