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Hydrazinecarboxamide, 2-[1-(3-fluorophenyl)ethylidene]-, is a chemical compound with the molecular formula C9H10FN3O. It is a derivative of hydrazinecarboxamide, featuring a 3-fluorophenyl group attached to an ethylidene moiety. Hydrazinecarboxamide, 2-[1-(3-fluorophenyl)ethylidene]- is known for its potential applications in pharmaceutical research, particularly as an intermediate in the synthesis of various medicinal agents. Its structure allows for the exploration of its properties and reactivity, which can be crucial in the development of new drugs. The presence of the fluorine atom in the phenyl ring can significantly influence the compound's pharmacokinetics and pharmacodynamics, making it an interesting candidate for further study in the field of drug design and development.

2968-03-8

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2968-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2968-03-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,6 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2968-03:
(6*2)+(5*9)+(4*6)+(3*8)+(2*0)+(1*3)=108
108 % 10 = 8
So 2968-03-8 is a valid CAS Registry Number.

2968-03-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-(3-fluorophenyl)ethylidene)hydrazinecarboxamide

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

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More Details:2968-03-8 SDS

2968-03-8Relevant academic research and scientific papers

Design and synthesis of amino acid derivatives of substituted benzimidazoles and pyrazoles as Sirt1 inhibitors

Asthana, Shailendra,Banerjee, Sanjay K.,Kumar, Vasantha,Paramesha, Bugga,Poojary, Boja,Purushotham, Nikil,Singh, Mrityunjay,Wakode, Sharad

, p. 3809 - 3827 (2022/02/16)

Owing to its presence in several biological processes, Sirt1 acts as a potential therapeutic target for many diseases. Here, we report the structure-based designing and synthesis of two distinct series of novel Sirt1 inhibitors, benzimidazole mono-peptide

Structure-activity relationship study of a novel necroptosis inhibitor, necrostatin-7

Zheng, Weihong,Degterev, Alexei,Hsu, Emily,Yuan, Junying,Yuan, Chengye

scheme or table, p. 4932 - 4935 (2009/05/26)

Necroptosis is a regulated caspase-independent cell death mechanism characterized by morphological features resembling non-regulated necrosis. Necrotatin-7 (Nec-7), a novel potent small-molecule inhibitor of necroptosis, is structurally distinct from previously described necrostatins (Nec-1, Nec-3, Nec-4 and Nec-5). Here, we describe a series of structural modifications and the structure-activity relationship (SAR) of the Nec-7 series for inhibiting necroptosis.

Synthesis of 3-substituted arylpyrazole-4-carboxylic acids

Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov

, p. 782 - 789 (2007/10/03)

A method was suggested for preparing previously unknown 3-aryl-substituted pyrazole-4-carboxylic acids, involving Vilsmeier formylation of semicarbazones of 26 available mono- and disubstituted acetophenones and 2-acetylthiophene followed by oxidation of

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