588678-04-0 Usage
General Description
The chemical 2,6-Dichloroprop-methyl ester, also known as dichlorprop-P, is an herbicide commonly used to control broadleaf weeds in various agricultural crops such as wheat, barley, and oats. It is a systemic herbicide, meaning it is absorbed and translocated throughout the plant, ultimately causing it to die. The ester form of dichlorprop-P is preferred for its ability to penetrate the waxy cuticle of the plant, allowing for better absorption and effectiveness. It works by disrupting the plant's hormonal balance and inhibiting its ability to grow and develop, ultimately leading to its death. However, dichlorprop-P is a highly toxic chemical and should be handled with caution, as it may have adverse effects on human health and the environment if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 588678-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,8,6,7 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 588678-04:
(8*5)+(7*8)+(6*8)+(5*6)+(4*7)+(3*8)+(2*0)+(1*4)=230
230 % 10 = 0
So 588678-04-0 is a valid CAS Registry Number.
588678-04-0Relevant articles and documents
Rac- and R-(+)-[4,4′,5,5′-2H4]-2- (1′-[2″,6″-dichlorophenoxy]-ethyl)-Δ2- imidazoline (lofexidine)
Vartak, Ashish P.,Sonar, Vijayakumar,Crooks, Peter A.
experimental part, p. 431 - 434 (2010/07/05)
The synthesis of the d4-forms of rac- and R-lofexidine was accomplished. Two methods are described; one method is a two-step synthesis of rac-d4-lofexidine from 2-chloropropionitrile, the second method is a three-step preparation of R-d4-lofexidine in absolute enantiomeric purity from S-methyl lactate. The commercial availability of R-methyl lactate makes this latter enantioselective synthesis applicable also to the synthesis of S-d4- lofexidine. These procedures also conserve the utilization of the relatively expensive [1,1′,2,2′-2H 4]ethylene diamine precursor. The availability of S- and R-d 4-lofexidines will enable pharmacokinetic studies to be carried out to determine if differential in vivo metabolism of the two enantiomers of lofexidine occurs. Copyright
