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3-(hydroxymethyl)-4-ketobenz-1,2,3-triazine is a heterocyclic compound characterized by a benzene ring fused to a triazine ring, featuring a hydroxymethyl group and a ketone group. 3-(hydroxymethyl)-4-ketobenz-1,2,3-triazine is recognized for its potential as a drug candidate in medicinal chemistry.
Used in Pharmaceutical Industry:
3-(hydroxymethyl)-4-ketobenz-1,2,3-triazine is used as a potential anti-cancer agent due to its ability to inhibit the growth of cancer cells. Its hydroxymethyl group offers a site for further chemical modifications and derivatization, which can enhance its bioactivity and selectivity for targeted cancer therapies.
Research on 3-(hydroxymethyl)-4-ketobenz-1,2,3-triazine is ongoing to explore its full potential in drug discovery and development, with a focus on its application in creating novel and effective cancer treatments.

24310-40-5

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24310-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24310-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,1 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24310-40:
(7*2)+(6*4)+(5*3)+(4*1)+(3*0)+(2*4)+(1*0)=65
65 % 10 = 5
So 24310-40-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3O2/c12-5-11-8(13)6-3-1-2-4-7(6)9-10-11/h1-4,12H,5H2

24310-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(hydroxymethyl)-1,2,3-benzotriazin-4-one

1.2 Other means of identification

Product number -
Other names 3-(hydroxymethyl)-1,2,3-benzotriazin-4(3H)-one

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:24310-40-5 SDS

24310-40-5Relevant academic research and scientific papers

Synthesis, antibacterial, and antiviral activities of novel penta-1,4-dien-3-one derivatives containing a benzotriazin-4(3H)-one moiety

Zhang, Ju-Ping,Li, Qin,Zhang, Cheng,Li, Pu,Chen, Li-Juan,Wang, Yi-Hui,Ruan, Xiang-Hui,Xiao, Wei,Xue, Wei

, p. 2193 - 2202 (2018)

A series of penta-1,4-dien-3-one containing a benzotriazin-4(3H)-one moiety were prepared and evaluated for their antibacterial and antiviral activities. Bioassays indicated that some compounds exhibited good antibacterial and antiviral activities. Among them, the EC50 values of compound 6d against Xanthomonas axonopodis pv. citri and compound 6l against Ralstonia solanacearum were, respectively, 22.45 and 34.77?μg/mL, which were better than that of thiodiazole copper (51.35 and 87.26?μg/mL, respectively). Meanwhile, some title compounds were found to show remarkable antiviral activities against tobacco mosaic virus (TMV). These results indicated that penta-1,4-dien-3-one derivatives containing benzotriazin-4(3H)-one moiety could play significant roles in searching for novel agrochemicals.

A benzene and three qinqin alkone of 1, 4 - pentadiene -3 - ketone derivatives, preparation method and use thereof

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Paragraph 0038; 0043, (2019/11/12)

The invention discloses a 1,4-pentadiene-3-ketone derivative containing benzotriazinone. The 1,4-pentadiene-3-ketone derivative containing benzotriazinone is characterized by having the general formula as shown in the specification, wherein R1 is phenyl, substituted phenyl (p-fluorophenyl, p-chlorophenyl, o-chlorophenyl, 2-methyoxyphenyl, 4-methyoxyphenyl, 4-methylphenyl, 2,4-dimethyoxyphenyl, 3,4-dimethyoxyphenyl, cinnamaldehyde group, 3-nitrophenyl, 2-chloro-5-nitrophenyl and the like), heterocyclic group (furyl, thienyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, pyrryl and the like) or substituted aromatic heterocyclic group (5-methyl thiazole, 5-methyl-2-thienyl, 4-bromo-2-thienyl and the like), and R2 is a hydrogen atom, methyl (ethyl), methoxyl (ethyoxyl) and the like. The compound disclosedby the invention has relatively high inhibiting activity for citrus canker bacteria, ralstonia solanacearum and tobacco mosaic viruses so as to be used for preparing an agricultural bactericide and anantiviral agent.

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