113036-88-7 Usage
Description
N-[[4-[[[(4-chlorophenyl)-cyclopropyl-methylidene]amino]oxymethyl]phenyl]carbamoyl]-2,6-difluoro-benzamide is a complex organic compound with a unique molecular structure. It is characterized by the presence of a cyclopropyl-methylidene group attached to a 4-chlorophenyl ring, which is connected to an aminooxymethyl group. N-[[4-[[[(4-chlorophenyl)-cyclopropyl-methylidene]amino]oxymethyl]phen yl]carbamoyl]-2,6-difluoro-benzamide also features a carbamoyl group linked to a 2,6-difluorobenzene ring. Its chemical properties and potential applications make it an interesting compound for various industries.
Uses
Used in Pharmaceutical Industry:
N-[[4-[[[(4-chlorophenyl)-cyclopropyl-methylidene]amino]oxymethyl]phenyl]carbamoyl]-2,6-difluoro-benzamide is used as a pharmaceutical compound for its potential therapeutic effects. Its unique molecular structure allows it to interact with specific biological targets, making it a promising candidate for the development of new drugs to treat various diseases.
Used in Agrochemical Industry:
In the agrochemical industry, N-[[4-[[[(4-chlorophenyl)-cyclopropyl-methylidene]amino]oxymethyl]phenyl]carbamoyl]-2,6-difluoro-benzamide is used as an insecticide and mite growth regulator. Its ability to inhibit chitin synthesis and regulate the growth of pests makes it an effective tool for controlling various agricultural pests, thereby protecting crops and increasing yield.
Used in Chemical Research:
N-[[4-[[[(4-chlorophenyl)-cyclopropyl-methylidene]amino]oxymethyl]phenyl]carbamoyl]-2,6-difluoro-benzamide is also used in chemical research as a starting material or intermediate for the synthesis of other complex organic compounds. Its unique structure and reactivity make it a valuable component in the development of new chemical processes and products.
Preparation
Flucycloxuron is produced by the reaction of 4-chlorocyclopropylphenone with hydroxylamine to yield the corresponding oxime, which is treated with 4-nitrobenzylbromide,followed by reduction to give the corresponding amine that is fur-ther treated with 2,6-difluorobenzoylisocyanate.
Toxicology
The WHO classifies flucycloxuron as a Class U toxin(unlikely to be hazardous). It is non-irritating to skin but mildly irritating to eyes. It is non-mutagenic, non-teratogenic and non-carcinogenic. The acute oral LD50, in rats is >5000 mg/kg.The acute dermal LD50 in rats is >2000 mg/kg.The NOEL inrats (2 year feed) is about 6 mg/kg/day.
Mode of action
Incorporation of N-acetylglucosamine into chitin was equally inhibited by flucycloxuron and diflubenzuron. Flucycloxuron has ovo-Iarvicidal activity (Grosscurt et al. 1988). Ir is non-systemic and has no activity on adults (Tomlin 1995).
Check Digit Verification of cas no
The CAS Registry Mumber 113036-88-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,3 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 113036-88:
(8*1)+(7*1)+(6*3)+(5*0)+(4*3)+(3*6)+(2*8)+(1*8)=87
87 % 10 = 7
So 113036-88-7 is a valid CAS Registry Number.
InChI:InChI=1/C25H20ClF2N3O3/c26-18-10-8-17(9-11-18)23(16-6-7-16)31-34-14-15-4-12-19(13-5-15)29-25(33)30-24(32)22-20(27)2-1-3-21(22)28/h1-5,8-13,16H,6-7,14H2,(H2,29,30,32,33)
