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Acetic acid, 2-cyano-, 2-[(2-hydroxyphenyl)methylene]hydrazide, also known as 2-cyano-2-[(2-hydroxyphenyl)methylene]hydrazide acetic acid, is a complex organic compound with the chemical formula C10H10N4O3. Acetic acid, 2-cyano-,2-[(2-hydroxyphenyl)methylene]hydrazide is characterized by its acetic acid backbone, which is substituted with a 2-cyano group and a 2-[(2-hydroxyphenyl)methylene]hydrazide moiety. The 2-hydroxyphenyl group introduces a hydroxyl functional group attached to a phenyl ring, which is further connected to a methylene bridge that leads to a hydrazide group. This molecule is of interest in chemical research and pharmaceutical development due to its potential applications in the synthesis of various compounds and its structural properties that may influence its reactivity and biological activity.

4974-49-6

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4974-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4974-49-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,7 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4974-49:
(6*4)+(5*9)+(4*7)+(3*4)+(2*4)+(1*9)=126
126 % 10 = 6
So 4974-49-6 is a valid CAS Registry Number.

4974-49-6SDS

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 2-cyano-N'-[(Z)-(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]acetohydrazide

1.2 Other means of identification

Product number -
Other names cyano-acetic acid salicylidenehydrazide

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:4974-49-6 SDS

4974-49-6Downstream Products

4974-49-6Relevant academic research and scientific papers

AIE based “on-off” fluorescence probe for the detection of Cu2+ ions in aqueous media

Assiri, Mohammed A.,Al-Sehemi, Abdullah G.,Pannipara, Mehboobali

, p. 11 - 15 (2019)

A simple hydrazine carboxamide derivative with intramolecular charge transfer and aggregation induced emission (AIE) properties have been designed and synthesized. The derivative (Probe 1) shows typical AIE characteristic emission in THF-water mixtures and emits yellowish orange color on reaching the water fraction 98%. The probe molecule show selective sensing response for Cu2+ ions via fluorescence turn-off mechanism in aqueous media over other metal ions. The emission changes towards Cu2+ ions that could be clearly observed by the naked eyes under 365 nm UV lamp promote the probe molecule as a promising candidate for practical utilization. Furthermore, from the fluorescence titration data, the detection limit for Cu2+ ions was found to be 0.44 μM.

Mechanistic differences between in vitro assays for hydrazone-based small molecule inhibitors of anthrax lethal factor

Hanna, M. Leslie,Tarasow, Theodore M.,Perkins, Julie

, p. 50 - 58 (2008/09/18)

A systematically generated series of hydrazones were analyzed as potential inhibitors of anthrax lethal factor. The hydrazones were screened using one UV-based and two fluorescence-based in vitro assays. The study identified several inhibitors with IC50 values in the micromolar range, and importantly, significant differences in the types of inhibition were observed with the different assays.

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