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178813-81-5

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178813-81-5 Usage

Description

FLUACRYPYRIM, a synthetic chemical compound, is primarily recognized for its potent pesticidal properties. It functions as a selective herbicide, effectively targeting and controlling a wide range of broadleaf and grassy weeds. FLUACRYPYRIM's mode of action involves inhibiting the enzyme protoporphyrinogen oxidase (PPO), which is essential for the synthesis of chlorophyll, ultimately leading to the weed's death. Additionally, it has been discovered to possess uterine relaxant, antinociceptive, and anti-inflammatory properties, making it a versatile compound with potential applications in various industries.

Uses

Used in Agricultural Industry:
FLUACRYPYRIM is used as a pesticide for its ability to control a broad spectrum of weeds, including broadleaf and grassy species. Its application in agriculture helps improve crop yield by reducing competition for resources and minimizing potential damage caused by weeds.
Used in Pharmaceutical Industry:
FLUACRYPYRIM is used as a uterine relaxant due to its ability to induce relaxation in the uterine muscles. This property makes it a potential candidate for the development of treatments for various gynecological conditions, such as dysmenorrhea and preterm labor.
FLUACRYPYRIM is also used for its antinociceptive and anti-inflammatory properties, which can be beneficial in the development of pain relief and anti-inflammatory medications. These applications can be particularly useful in managing conditions like arthritis, muscle pain, and other inflammatory disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 178813-81-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,8,1 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 178813-81:
(8*1)+(7*7)+(6*8)+(5*8)+(4*1)+(3*3)+(2*8)+(1*1)=175
175 % 10 = 5
So 178813-81-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H21F3N2O5/c1-12(2)30-19-24-16(20(21,22)23)9-17(25-19)29-10-13-7-5-6-8-14(13)15(11-27-3)18(26)28-4/h5-9,11-12H,10H2,1-4H3/b15-11+

178813-81-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name FLUACRYPYRIM

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:178813-81-5 SDS

178813-81-5Downstream Products

178813-81-5Relevant articles and documents

Process for producing acrylic acid derivative

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Page 34, (2010/02/08)

Processes for producing a compound represented by the formula (1), which includes an acrylic acid derivative and is useful as an agricultural chemical or medicine. One of the processes comprises the step of formulating a compound (3) and converting the OH of the resultant compound (2) into OR″. The first step comprises reacting a formic or orthoformic ester in the presence of a Lewis acid and a base. The second step comprises reacting the compound with R″OH or with R″OH and CH(OR″)3 under acidic conditions or using a phase-transfer catalyst in a two-phase system and regulating the base and the concentration thereof to stereoselectively synthesize the target compound. In another, process, the compound is efficiently produced without isolating the compound. The compound can also be produced without the compound (2).

PROCESSES FOR PRODUCING ACRYLIC ACID DERIVATIVE

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, (2008/06/13)

Processes for producing a compound (1) represented by formula (1), which includes an acrylic acid derivative and is useful as an agricultural chemical or medicine. One of the processes comprises the step of formylating a compound (3) (step (1)) and the step of converting the OH of the resultant compound (2) into OR" (step (2)). The step (1) comprises reacting a formic or orthoformic ester in the presence of a Lewis acid and a base. The step (2) comprises [1] reacting the compound (2) with R" OH or with R" OH and CH(OR")3under acidic conditions or [2] using a phase-transfer catalyst in a two-phase system and regulating the base and the concentration thereof to stereoselectively synthesize the target compound. In another process, the compound (1) is efficiently produced without isolating the compound (2). In still another process, the compound (1) is directly produced without via the compound (2).

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