38580-89-1 Usage
Uses
Used in Agricultural Industry:
Isopropyl dimethylcarbamate is used as an insecticide for pest control, specifically targeting insects that are detrimental to crops. Its application is aimed at protecting agricultural yields by reducing the impact of insect pests.
Used in Household Pest Control:
IPDC is used as a household insecticide for controlling common pests such as ants, cockroaches, and bedbugs. It is valued for its effectiveness in eliminating these pests, thereby improving the cleanliness and safety of living environments.
Used in Head Lice Treatment:
Isopropyl dimethylcarbamate is used as an active ingredient in treatments for head lice infestations. Its role in these treatments is to eliminate the lice and reduce the discomfort and health risks associated with infestations.
Check Digit Verification of cas no
The CAS Registry Mumber 38580-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,5,8 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38580-89:
(7*3)+(6*8)+(5*5)+(4*8)+(3*0)+(2*8)+(1*9)=151
151 % 10 = 1
So 38580-89-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2/c1-5(2)9-6(8)7(3)4/h5H,1-4H3
38580-89-1Relevant academic research and scientific papers
A formal synthesis of optically active clavicipitic acids, unusual azepinoindole-type ergot alkaloids
Shinohara, Hirofumi,Fukuda, Tsutomu,Iwao, Masatomo
, p. 10989 - 11000 (2007/10/03)
An enantioselective synthesis of (-)-cis, and (-)-trans-clavicipitic acid methyl esters (15a,b) has been achieved. The key steps of the synthesis were 1) C-4 selective functionalization of the indole ring via directed lithiation of I-(triisopropylsilyl)gramine (2), and 2) stereoselective alkylation of the lithiated (2R)-(-)-2,5-dihydro-2-isopropyl-3,6- dimethoxypyrazine (Schoollkopf's bislactim ether) (4) with 1-l- butoxycarbonyl-3-chloromethyl-4-[(E)-3-methoxy-3-methyl-1-butenyllindole (10). The diastereoselectivity of the latter reaction was found to be highly dependent on the coordinating ability of solvents or additives. The optically active amino-alcohol 13, prepared by the mild acid hydrolysis of the alkylation product 11a, was successfully convened to the azepinoindoles 14a, b by PPTS-catalyzed dehydrative cyclization. During the course of the final deprotection of N-Boc group, an interesting cis-trans isomerization between 15a and 15b, which proceeded via acid-catalyzed ring opening and recyclization at C-6, was observed.
