3290-01-5 Usage
Description
2,3-Dichlorobenzyl chloride is a clear colorless liquid that serves as a versatile chemical intermediate in the synthesis of various compounds. It is characterized by its chemical structure, which includes two chlorine atoms attached to the benzene ring, specifically at the 2nd and 3rd positions, and a reactive chlorine atom attached to the benzyl group.
Uses
Used in the Chemical Industry:
2,3-Dichlorobenzyl chloride is used as a chemical intermediate for the preparation of Biquaternary Ammonium compounds. These compounds are essential in various applications, such as pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in the Agricultural Industry:
2,3-Dichlorobenzyl chloride is also used in the preparation of substituted Aryland Heteroarylcarboxylic Acid Hydrazides and their salts. These compounds are known to increase stress tolerance in plants, making them more resilient to environmental challenges such as drought, salinity, and extreme temperatures. This application can lead to improved crop yields and better adaptation to changing climate conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 3290-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3290-01:
(6*3)+(5*2)+(4*9)+(3*0)+(2*0)+(1*1)=65
65 % 10 = 5
So 3290-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H5Cl3/c8-4-5-2-1-3-6(9)7(5)10/h1-3H,4H2
3290-01-5Relevant articles and documents
Antihypertensive Activity of 6-Arylpyridopyrimidin-7-amine Derivatives
Bennett, Lawrence R.,Blankley, C. John,Fleming, Robert W.,Smith, Ronald D.,Tessman, Deirdre K.
, p. 382 - 389 (2007/10/02)
A series of 51 6-arylpyridopyrimidin-7-amine derivatives was prepared and evaluated for antihypertensive activity in the conscious spontaneously hypertensive rat.A number of these compounds, notably 6-(2,6-dichlorophenyl)-2-methylpyridopyrimidin-7-amine (36), lowered blood pressure in these rats in a gradual and sustained manner to normotensive levels at oral doses of 10-50 mg/kg.Normalized blood pressure levels could then be maintained by single daily oral doses.The effect of structural variation in the 6-aryl group and in the 2 and 4 positions of the pyridopyrimidine ring on activity is reported and discussed.
