95977-29-0 Usage
Description
Haloxyfop-P is a synthetic auxin herbicide that selectively controls broadleaf and grassy weeds in various crops. It works by mimicking the action of natural plant hormones, causing uncontrolled growth and eventually leading to the death of the targeted weeds. Its selective action and effectiveness make it a valuable tool in modern agriculture for maintaining crop yields and quality.
Uses
Used in Agriculture:
Haloxyfop-P is used as a herbicide for controlling a wide range of broadleaf and grassy weeds in various crops, including cassia fields. Its application helps to protect the crops from competition and damage caused by these weeds, ensuring healthy growth and higher yields.
Used in Cassia Fields:
Specifically in cassia fields, Haloxyfop-P is used as a selective herbicide to control weeds that may compete with cassia plants for nutrients, water, and sunlight. By eliminating these weeds, the herbicide promotes the growth and development of cassia plants, leading to a more productive and profitable harvest.
As a Pesticide Residue in Vegetables:
While Haloxyfop-P is primarily used in non-crop areas or in crops like cassia, it is also important to monitor its residues in vegetables to ensure food safety. This involves setting maximum residue limits (MRLs) and conducting regular testing to prevent any potential health risks associated with the consumption of contaminated produce.
Check Digit Verification of cas no
The CAS Registry Mumber 95977-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,9,7 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95977-29:
(7*9)+(6*5)+(5*9)+(4*7)+(3*7)+(2*2)+(1*9)=200
200 % 10 = 0
So 95977-29-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H11ClF3NO4/c1-8(14(21)22)23-10-2-4-11(5-3-10)24-13-12(16)6-9(7-20-13)15(17,18)19/h2-8H,1H3,(H,21,22)/t8-/m1/s1
95977-29-0Relevant articles and documents
Structure, activity, and inhibition of the carboxyltransferase β-Subunit of acetyl coenzyme a carboxylase (AccD6) from mycobacterium tuberculosis
Reddy, Manchi C.M.,Breda, Ardala,Bruning, John B.,Sherekar, Mukul,Valluru, Spandana,Thurman, Cory,Ehrenfeld, Hannah,Sacchettini, James C.
, p. 6122 - 6132 (2014)
In Mycobacterium tuberculosis, the carboxylation of acetyl coenzyme A (acetyl-CoA) to produce malonyl-CoA, a building block in long-chain fatty acid biosynthesis, is catalyzed by two enzymes working sequentially: a biotin carboxylase (AccA) and a carboxyl
Synthesis and herbicidal activity of 2-(4-aryloxyphenoxy)propionamides
Hui, Yang Zi
, p. 385 - 387 (2018/09/29)
Two novel 2-(4-aryloxyphenoxy)propionamide derivatives were synthesized based on the structure of metamifop. Their structures were confirmed by 1H nuclear magnetic resonance, elemental analysis, and optical rotation. The preliminary bioassay re
Tetrahydro naphthalene-2-aryloxy phenoxy alkyl ketone compound with anti-tumor activity and pharmaceutical application of compound
-
Paragraph 0019; 0020; 0021, (2018/09/11)
The invention discloses a tetrahydro naphthalene-2-aryloxy phenoxy alkyl ketone compound and a medical application thereof. The chemical structural formula of the compound is as shown in the formula Iin the specification, wherein R1, R2, R3 and R4 are any
