76502-61-9 Usage
Uses
Used in Pharmaceutical Industry:
3-Chlorobenzyl urea is used as a key intermediate in the synthesis of various pharmaceuticals for its potential as an anti-cancer agent. It contributes to the development of drugs that target cancer cells and may have applications in treating a range of malignancies.
Used in Agrochemical Industry:
3-Chlorobenzyl urea is used as an active ingredient in the development of insecticides and herbicides due to its insecticidal and herbicidal properties. It helps in controlling pests and weeds, thereby enhancing crop productivity and protecting agricultural yields.
Used in Research and Development:
3-Chlorobenzyl urea is utilized as a building block in the preparation of biologically active compounds for research purposes. Its unique structure and properties make it a promising candidate for the discovery of new drugs and agrochemicals with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 76502-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,0 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76502-61:
(7*7)+(6*6)+(5*5)+(4*0)+(3*2)+(2*6)+(1*1)=129
129 % 10 = 9
So 76502-61-9 is a valid CAS Registry Number.
76502-61-9Relevant academic research and scientific papers
Kinetics and mechanism of the aminolysis of aryl thiocarbamates: Effects of the non-leaving group
Oh, Hyuck Keun,Jin, Young Cheul,Sung, Dae Dong,Lee, Ikchoon
, p. 1240 - 1244 (2007/10/03)
The kinetics of the aminolysis of aryl thiocarbamates [ATC: H 2NC(=O)SC6H4Z] with benzylamines (XC 6H4CH2NH2) in acetonitrile at 10.0°C have been studied. The rate order with variation of the non-leaving amino group, RNH, in RNHC(=O)SC6H4Z is NH2 s) effects of the RNH group are insignificant, and the strength of push to expel the leaving group in the tetrahedral transition state is the sole, important effect. The strong push provided by the NH2 group, the negative ρxz (-0.38) value, the size of βz (-0.54), and failure of the reactivity-selectivity principle are all consistent with the concerted mechanism. The kinetic isotope effects involving deuterated amine nucleophiles (XC6H4CH2ND2) are normal (kH/kD ≈ 1.40-1.73) suggesting a hydrogen-bonded cyclic transition state. The Royal Society of Chemistry 2005.
Aryl thioxanthines
-
, (2008/06/13)
PCT No. PCT/US95/16723 Sec. 371 Date Aug. 18, 1997 Sec. 102(e) Date Aug. 18, 1997 PCT Filed Dec. 12, 1995 PCT Pub. No. WO96/18399 PCT Pub. Date Jun. 20, 1996The present invention relates to novel compounds of the formula (I): wherein Q3R3 and Q8R8 are des
