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Benzoic acid 2-propylhydrazide is an organic compound with the chemical formula C10H12N2O2. It is a derivative of benzoic acid, where the carboxylic acid group is replaced by a hydrazide group, specifically a 2-propyl group attached to the hydrazide. Benzoic acid, 2-propylhydrazide is white to off-white in color and is soluble in organic solvents. It is used in the synthesis of various pharmaceuticals and as an intermediate in chemical reactions. Due to its reactivity, it is important to handle it with care, following proper safety protocols.

7696-84-6

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7696-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7696-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,9 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7696-84:
(6*7)+(5*6)+(4*9)+(3*6)+(2*8)+(1*4)=146
146 % 10 = 6
So 7696-84-6 is a valid CAS Registry Number.

7696-84-6Downstream Products

7696-84-6Relevant academic research and scientific papers

Iminium ion catalysis: Use of the α-effect in the acceleration of the Diels-Alder reaction

Cavill, Julie L.,Peters, Jens-Uwe,Tomkinson, Nicholas C. O.

, p. 728 - 729 (2003)

The α-effect can be used in the acceleration of the DielsAlder reaction between a series of dienes and electron deficient dienophiles using iminium ion catalysis, providing a novel molecular scaffold capable of performing this class of catalytic process.

Synthesis of N′-propylhydrazide analogs of hydroxamic inhibitors of histone deacetylases (HDACs) and evaluation of their impact on activities of HDACs and replication of hepatitis C virus (HCV)

Kozlov, Maxim V.,Konduktorov, Konstantin A.,Shcherbakova, Anastasia S.,Kochetkov, Sergey N.

supporting information, p. 2369 - 2374 (2019/06/17)

N′-Propylhydrazide analogs of hydroxamic inhibitors of histone deacetylases (HDACs), including tubastatin A, vorinostat and belinostat, were synthesized. All prepared compounds inhibited HDAC1/2/3, but not HDAC6, except for one hydrazide analog of HDAC4/5/7 inhibitor that was completely inactive. A novel 4-substituted derivative of N′-propylbenzohydrazide with extremely high anti-HCV activity was discovered.

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