66410-68-2 Usage
Uses
Used in Pharmaceutical Synthesis:
MD-Chloride is used as a reagent in the pharmaceutical industry for the synthesis of various compounds. Its unique chemical structure allows it to be a versatile building block in the creation of new drugs, contributing to the development of novel therapeutic agents.
Used in Agrochemical Production:
In the agrochemical sector, MD-Chloride is utilized in the production of pesticides and insecticides. Its reactivity and ability to form stable bonds with other molecules make it an essential component in the formulation of effective crop protection products.
Used in Organic Compound Manufacturing:
MD-Chloride also serves as a key intermediate in the manufacturing of certain organic compounds. Its presence in the synthesis process is crucial for achieving the desired chemical properties and functionalities of the final product.
Safety Precautions:
Given the toxic nature of MD-Chloride, it is imperative to handle 3,4-DIHYDRO-2H-1,5-BENZODIOXEPINE-6-CARBONYL CHLORIDE with extreme caution. Proper protective equipment, such as gloves, goggles, and respiratory masks, should be worn during its use to minimize the risk of skin, eye, and respiratory irritation. Additionally, handling should be conducted in a well-ventilated area to reduce the potential for harmful vapor exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 66410-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,1 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66410-68:
(7*6)+(6*6)+(5*4)+(4*1)+(3*0)+(2*6)+(1*8)=122
122 % 10 = 2
So 66410-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClO3/c11-10(12)7-3-1-4-8-9(7)14-6-2-5-13-8/h1,3-4H,2,5-6H2
66410-68-2Relevant academic research and scientific papers
Substituted 2,3-alkylene bis (oxy) benzamides and derivatives and method of preparation
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, (2008/06/13)
Novel substituted 2,3-alkylene bis (oxy) benzamides and derivatives thereof are disclosed. Also disclosed is a method for producing said compounds. The compounds have anxiolytic, psychostimulant, disinhibiting and thymoanaleptic properties useful therapeutically in the psychofunctional field, particularly in gastro-enterology, cardiology, urology, rheumatology and gynaecology.
