91012-53-2 Usage
Description
(N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHENOXYMETHANE, commonly known as Methomyl, is an organophosphate insecticide and acaricide used in agriculture to control pests such as aphids, thrips, and mites in crops like cotton, fruit trees, and vegetables. It functions as a cholinesterase inhibitor, disrupting the nervous system of insects and leading to paralysis and death.
Used in Agricultural Industry:
(N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHENOXYMETHANE is used as an insecticide and acaricide for controlling a wide variety of pests in crops such as cotton, fruit trees, and vegetables. It is effective in managing insects like aphids, thrips, and mites, which can cause significant damage to these crops.
However, it is important to note that Methomyl is toxic to humans and other non-target organisms, and its use has been restricted in some countries due to potential ecological and health risks. Exposure to Methomyl can cause symptoms such as nausea, vomiting, diarrhea, and headaches, and it has been classified as a likely human carcinogen. As a result, alternative pest control methods and safer insecticides are being sought to minimize these risks.
Check Digit Verification of cas no
The CAS Registry Mumber 91012-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,1 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91012-53:
(7*9)+(6*1)+(5*0)+(4*1)+(3*2)+(2*5)+(1*3)=92
92 % 10 = 2
So 91012-53-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3/c1-11(13-2)10(12)8-14-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3
91012-53-2Relevant articles and documents
ANTIINFLAMMATORY AND ANTITUMOR 2-OXOTHIAZOLES AND 2-OXOTHIOPHENES COMPOUNDS
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, (2014/08/19)
A compound of formula (I) wherein X is O, C O or S; Y is N or CH; R2 and R4 are each independently H, -(CH2)pCOOH, -(CH2)pCON(R5)2 or - (CH2)pCOOC 1-6alkyI; or R2 and R4 together form a 6-membered phenyl ring fused to the five membered ring; each R1 is independently selected from H, halo (e.g. fluoro or chloro), C6-10aryl, C7-12arylalkyl, C2-12alkenyl; OC1-2 alkyl, OC2-12 aikenyl or a C1-12 alkyl group; each R5 is H or C1-6 alkyl; each p is 0 to 3; n is 1 to 4; or a salt, ester, solvate, N-oxide, or prodrug thereof, e.g. a salt thereof.
NEW ROUTES TO TRANS A,B-SUBSTITUTED BACTERIOCHLORINS
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Page/Page column 79, (2013/05/21)
Bacteriochlorin of Formula I: wherein R is H or silyl are described, along with compositions containing the same and methods of making and using the same.
A method for the synthesis of cyclopropanes by regiospecific and regioselective magnesium carbenoid 1, 3-CH insertion as the key reactions
Watanabe, Hiroyuki,Ogata, Shingo,Satoh, Tsuyoshi
experimental part, p. 5675 - 5686 (2010/11/24)
Addition reaction of two geometrical isomers of 1-chlorovinyl p-tolyl sulfoxides derived from unsymmetrical ketones and chloromethyl p-tolyl sulfoxide, with lithium enolate of tert-butyl acetate gave single diastereomers of the adduct, respectively. Treat
