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17372-26-8

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17372-26-8 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This is the IUPAC name of the compound, which describes the structure and composition of the molecule.

Explanation

The compound is used as a reducing agent in organic chemistry reactions, which means it donates electrons to other molecules.

Explanation

The compound is used in the preparation of various chemical substances, including those used in the pharmaceutical, agrochemical, and plastic industries.

Explanation

The compound plays a crucial role in the synthesis of various complex organic molecules, which are essential for the development of new materials and products.

Explanation

The compound acts as a catalyst in the production of fine chemicals, which are high-purity chemicals used in various industries.

Explanation

The compound is used as a reagent in the synthesis of heterocyclic compounds, which are organic compounds containing a ring of atoms with at least one heteroatom (e.g., nitrogen, oxygen, or sulfur).

Explanation

The compound has a variety of industrial applications and is commonly used in the manufacturing industry for the production of various products and materials.

Explanation

The compound carries a negative charge of -1, indicating that it is an anion.

Explanation

The compound is soluble in water and various organic solvents, which makes it suitable for use in a wide range of chemical reactions and processes.

Type of Compound

Reducing agent

Applications

Pharmaceutical, agrochemical, and plastic synthesis

Role in Synthesis

Key component in the synthesis of complex organic molecules

Use as a Catalyst

Production of fine chemicals

Use as a Reagent

Synthesis of heterocyclic compounds

Industrial Applications

Widely used in the manufacturing industry

Charge

Ion(1-)

Solubility

Soluble in water and organic solvents

Check Digit Verification of cas no

The CAS Registry Mumber 17372-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,7 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17372-26:
(7*1)+(6*7)+(5*3)+(4*7)+(3*2)+(2*2)+(1*6)=108
108 % 10 = 8
So 17372-26-8 is a valid CAS Registry Number.

17372-26-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium enolate of dimedone

1.2 Other means of identification

Product number -
Other names dimedone sodium enolate

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:17372-26-8 SDS

17372-26-8Upstream product

17372-26-8Relevant articles and documents

Norbornene probes for the study of cysteine oxidation

Alcock, Lisa J.,Farrell, Kyle D.,Akol, Mawey T.,Jones, Gregory H.,Tierney, Matthew M.,Kramer, Holger B.,Pukala, Tara L.,Bernardes, Gon?alo J.L.,Perkins, Michael V.,Chalker, Justin M.

, p. 1220 - 1228 (2018)

Cysteine residues on proteins can react with cellular oxidants such as hydrogen peroxide. While this process is important for scavenging excess reactive oxygen species, the products of this oxidation may also mediate cell signalling. To understand the role of cysteine oxidation in biology, selective probes are required to detect and quantify its occurrence. Cysteine oxidation products such as sulfenic acids are sometimes unstable and therefore short-lived. If such cysteine derivatives are to be analysed, rapid reaction with the probe is required. Here we introduce norbornene derivatives as probes for cysteine oxidation, and demonstrate their ability to trap sulfenic acids. The synthesis of norbornene derivatives containing alkyne or biotin affinity tags are also reported to facilitate the use of these probes in chemical biology and proteomics.

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