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Benzoic acid, 4-[(1-chloro-2-ethoxy-2-oxoethylidene)hydrazino]-, ethyl ester is a complex organic compound that features a benzoic acid group and an ethyl ester group, with a hydrazino functional group attached to the benzoic acid. Additionally, it incorporates a chloro and ethoxy groups linked to the hydrazino moiety. This chemical is primarily utilized in the synthesis of pharmaceuticals and for research purposes in the chemical industry, holding promise for the development of new medications and treatments for a range of diseases and conditions. Due to its potential reactivity and toxicity, it is crucial to handle this chemical with care and adhere to proper safety protocols.

105151-80-2

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105151-80-2 Usage

Uses

Used in Pharmaceutical Synthesis:
Benzoic acid, 4-[(1-chloro-2-ethoxy-2-oxoethylidene)hydrazino]-, ethyl ester is employed as a key intermediate in the synthesis of various pharmaceuticals for its unique structural features that can be further modified to create active drug molecules.
Used in Chemical Research:
In the realm of chemical research, Benzoic acid, 4-[(1-chloro-2-ethoxy-2-oxoethylidene)hydrazino]-, ethyl ester serves as a valuable subject for studying the properties and reactions of complex organic molecules, contributing to the advancement of organic chemistry and the discovery of new chemical reactions and processes.
Used in Medication Development:
Benzoic acid, 4-[(1-chloro-2-ethoxy-2-oxoethylidene)hydrazino]-, ethyl
ester is utilized in the development of medications, potentially leading to the creation of new treatments for various diseases and conditions. Its unique structure allows for the exploration of its therapeutic potential and its integration into novel drug candidates.
Used in Application Industry:
Benzoic acid, 4-[(1-chloro-2-oxoethylidene)hydrazino]-, ethyl ester is used as a chemical building block in the application industry for the synthesis of specialty chemicals and materials that may have specific uses depending on the industry's requirements.

Check Digit Verification of cas no

The CAS Registry Mumber 105151-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,1,5 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105151-80:
(8*1)+(7*0)+(6*5)+(5*1)+(4*5)+(3*1)+(2*8)+(1*0)=82
82 % 10 = 2
So 105151-80-2 is a valid CAS Registry Number.

105151-80-2Downstream Products

105151-80-2Relevant academic research and scientific papers

Kinetics and mechanism of dehydrochlorination of N-aryl-C-ethoxycarbonylformohydrazidoyl chlorides

Shawali, Ahmad S.,Albar, Hassan A.

, p. 871 - 875 (2007/10/02)

The kinetics of triethylamine (TEA) catalyzed dehydrochlorination of a series of N-aryl-C-ethoxycarbonylformohydrazidoyl chlorides 1a-m have been studied under pseudo-first-order conditions in 4:1 (v/v) dioxane-water solution at 30 deg C.For all compounds

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