52427-09-5 Usage
Description
(2-hydroxy-5-nitro-phenoxy)-acetic acid, also known as 2-hydroxy-5-nitrophenoxyacetic acid, is a chemical compound with the molecular formula C8H7NO6. It is a nitrophenyl derivative of acetic acid, characterized by its potential to control a range of broadleaf weeds and grasses.
Used in Agricultural Industry:
(2-hydroxy-5-nitro-phenoxy)-acetic acid is used as a herbicide for controlling a range of broadleaf weeds and grasses. It inhibits the growth of unwanted plants by disrupting their natural processes, making it a popular choice for agricultural applications.
Used in Industrial Applications:
In the industrial sector, (2-hydroxy-5-nitro-phenoxy)-acetic acid is utilized as a herbicide to manage unwanted plant growth in various settings. Its effectiveness in controlling a broad spectrum of weeds and grasses contributes to its popularity in this field.
Note: It is crucial to handle (2-hydroxy-5-nitro-phenoxy)-acetic acid with care due to its potential toxicity to humans and other living organisms if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 52427-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,2 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52427-09:
(7*5)+(6*2)+(5*4)+(4*2)+(3*7)+(2*0)+(1*9)=105
105 % 10 = 5
So 52427-09-5 is a valid CAS Registry Number.
52427-09-5Relevant articles and documents
Engineering Orthogonal Methyltransferases to Create Alternative Bioalkylation Pathways
Bennett, Matthew R.,Cronin, Victoria A.,Herbert, Abigail J.,Micklefield, Jason,Shepherd, Sarah A.,Sung, Rehana
supporting information, p. 14950 - 14956 (2020/07/04)
S-adenosyl-l-methionine (SAM)-dependent methyltransferases (MTs) catalyse the methylation of a vast array of small metabolites and biomacromolecules. Recently, rare carboxymethylation pathways have been discovered, including carboxymethyltransferase enzymes that utilise a carboxy-SAM (cxSAM) cofactor generated from SAM by a cxSAM synthase (CmoA). We show how MT enzymes can utilise cxSAM to catalyse carboxymethylation of tetrahydroisoquinoline (THIQ) and catechol substrates. Site-directed mutagenesis was used to create orthogonal MTs possessing improved catalytic activity and selectivity for cxSAM, with subsequent coupling to CmoA resulting in more efficient and selective carboxymethylation. An enzymatic approach was also developed to generate a previously undescribed co-factor, carboxy-S-adenosyl-l-ethionine (cxSAE), thereby enabling the stereoselective transfer of a chiral 1-carboxyethyl group to the substrate.
