2114-20-7 Usage
Uses
Used in Pesticide Production:
Carbamic acid hexyl ester is used as an active ingredient in the formulation of pesticides, contributing to the control of pests and insects in agricultural settings. Its carbamate nature allows it to target the nervous systems of pests, leading to paralysis and death.
Used in Fungicide Production:
Carbamic acid hexyl ester is used as a component in fungicides, helping to protect crops from fungal infections and diseases. Its effectiveness in inhibiting fungal growth makes it a valuable addition to agricultural protection strategies.
Used in Herbicide Production:
Carbamic acid hexyl ester is used as a key component in herbicides, aiding in the control of unwanted plant growth in agricultural fields and other areas. Its ability to target and inhibit plant growth makes it a useful tool in maintaining healthy and productive crops.
Used in Pharmaceutical Development:
Carbamic acid hexyl ester is used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its carbamate structure provides a versatile platform for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
Carbamic acid hexyl ester is used as a research compound in the study of carbamate chemistry and its potential applications in various fields. Its unique properties and reactivity make it an interesting subject for scientific investigation and discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 2114-20-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2114-20:
(6*2)+(5*1)+(4*1)+(3*4)+(2*2)+(1*0)=37
37 % 10 = 7
So 2114-20-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO2/c1-2-3-4-5-6-10-7(8)9/h2-6H2,1H3,(H2,8,9)
2114-20-7Relevant academic research and scientific papers
Indium(III)-Catalyzed Synthesis of Primary Carbamates and N-Substituted Ureas
Jain, Isha,Malik, Payal
supporting information, p. 93 - 97 (2021/11/26)
An indium triflate-catalyzed synthesis of primary carbamates from alcohols and urea as an ecofriendly carbonyl source has been developed. Various linear, branched, and cyclic alcohols were converted into the corresponding carbamates in good to excellent yields. This method also provided access to N-substituted ureas by carbamoylation of amines. All the products were obtained by simple filtration or crystallization, without the need for chromatographic purification. Mechanistic investigations suggest that the carbamoylation reaction proceeds through activation of urea by O-coordination with indium, followed by nucleophilic attack by the alcohol or amine on the carbonyl center of urea. The inexpensive and easily available starting materials and catalyst, the short reaction times, and the ease of product isolation highlight the inherent practicality of the developed method.
NOVEL KLK4 INHIBITORS
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Page/Page column 32; 33, (2015/12/18)
The present invention relates to novel compounds and probes which have a common chemical structure necessary to obtain potent inhibitory activity against KLK4 and/or may be used for the detection of KLK4 peptides and their activity. It further relates to the use of these compounds and methods for inhibiting and/or detecting KLK4 activity in vitro and in vivo by making use of said probes or inhibitors. The compounds of the invention differ from prior art compounds at least in the presence of phenyl guanidine (instead of e.g. benzyl guanidine) and/or the presence of a heteroatom in the tail group, their combined presence unexpectedly leading to potent and selective KLK4 inhibitory activity.
