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25141-25-7

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25141-25-7 Usage

General Description

2-(2,4-dinitrophenoxy)acetic acid, also known as dinoseb, is a synthetic organic compound that is commonly used as a herbicide. It is a derivative of acetic acid and contains two nitro groups and a phenoxy group. Dinoseb is known for its effectiveness in controlling a wide variety of broadleaf weeds, making it a popular choice for agricultural and gardening purposes. However, it is also classified as a highly toxic substance and is considered a potential health hazard, with potential risks of skin irritation, respiratory issues, and central nervous system effects if exposure levels are not properly controlled. Due to its hazardous nature, its use has been significantly restricted in many countries.

Check Digit Verification of cas no

The CAS Registry Mumber 25141-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,4 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25141-25:
(7*2)+(6*5)+(5*1)+(4*4)+(3*1)+(2*2)+(1*5)=77
77 % 10 = 7
So 25141-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O7/c11-8(12)4-17-7-2-1-5(9(13)14)3-6(7)10(15)16/h1-3H,4H2,(H,11,12)

25141-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,4-dinitrophenoxy)acetic acid

1.2 Other means of identification

Product number -
Other names 2.4-Dinitro-phenylaetherglykolsaeure

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:25141-25-7 SDS

25141-25-7Relevant articles and documents

EGFR-targeting fluorescence quenching probe and preparation method and application thereof

-

, (2020/12/09)

The invention relates to the technical field of molecular probes, and discloses an EGFR-targeting fluorescence quenching probe and a preparation method and application thereof. The fluorescence quenching probe structurally comprises a pharmacodynamic skeleton structure, a fluorescence quenching group and a fluorescence labeling group, wherein the fluorescence labeling group is selected from BODIPYFL dye; and the fluorescence quenching group is selected from 2, 4-dinitrophenol. The pharmacodynamic skeleton structure can be combined with EGFR protein in a targeting mode, and when the quenchinggroup in the molecular probe leaves, the fluorescence labeling group can conduct specific tracing and imaging; and by means of molecular imaging, the expression process of specific cells and moleculescan be observed in real time, a target spot is traced, and therefore disease development status evaluation and accurate detection of EGFR mutation typing of lung cancer patients are achieved at the molecular pathological level.

Synthesis of some new bio-active aryl amides

Srivastava,Purohit,Srivastava,Jain,Khubchandani

, p. 358 - 359 (2007/10/02)

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