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7253-59-0

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7253-59-0 Usage

Molecular structure

A hydrazine group attached to a carboxybenzylidene group, both connected to a trimethyl-2-oxoethanaminium moiety.

Type of compound

Quaternary ammonium salt, containing four carbon atoms bonded to a positively charged nitrogen atom.

Potential applications

Medicinal and pharmaceutical chemistry due to the presence of the carboxybenzylidene group, which can form a Schiff base with various biological molecules.

Utility as a cationic surfactant

The quaternary ammonium salt structure makes it a potential candidate for use as a cationic surfactant or stabilizer in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7253-59-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7253-59:
(6*7)+(5*2)+(4*5)+(3*3)+(2*5)+(1*9)=100
100 % 10 = 0
So 7253-59-0 is a valid CAS Registry Number.

7253-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[(2Z)-2-[(2-carboxyphenyl)methylidene]hydrazinyl]-2-oxoethyl]-trimethylazanium,chloride

1.2 Other means of identification

Product number -
Other names -

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:7253-59-0 SDS

7253-59-0Downstream Products

7253-59-0Relevant articles and documents

Enhancing the kinetics of hydrazone exchange processes: An experimental and computational study

Higgs, Patrick L.,Ruiz-Sanchez, Antonio J.,Dalmina, Milene,Horrocks, Benjamin R.,Leach, Andrew G.,Fulton, David A.

supporting information, p. 3218 - 3224 (2019/03/26)

The capacity of hydrazone bonds to readily undergo component exchange processes sees their extensive utilization in dynamic combinatorial chemistry. The kinetics of hydrazone exchange are optimal at pH ~4.5, which limits the use of hydrazone-based dynamic combinatorial libraries, particularly for biological targets which are only stable at near-neutral pH values. It would thus be advantageous if hydrazone exchange proceeded with faster rates at pH values closer to neutral. We experimentally and computationally evaluated the hypothesis that hydrazones possessing neighbouring acidic or basic functional groups within the carbonyl-derived moitety of the hydrazone would enhance exchange rates. Our work suggests that judiciously placed N- or O-hydrogen bond acceptors within the carbonyl-derived moiety of the hydrazone stabilize transition states via hydrogen bonding interactions, providing a valuable boost to exchange kinetics at near-neutral pH values. We anticipate these findings will be of interest in dynamic combinatorial chemistry, dynamic covalent polymers/materials, functionalized nanoparticles and interlocked molecules, all of which may benefit from hydrazone exchange processes able to operate at near-neutral pH values.

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