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1-Benzyl-2-methyl-1,2-dihydro-indazol-3-one is a chemical compound belonging to the indazole family, characterized by a fused indole and pyrazole ring system. This specific compound features a benzyl group attached to the nitrogen atom at position 1 and a methyl group at position 2, with the entire structure being a dihydro derivative, meaning it contains one less double bond than the parent indazole. The 3-one functional group indicates the presence of a carbonyl group at position 3, which is crucial for its reactivity and potential applications in various chemical and pharmaceutical processes. 1-benzyl-2-methyl-1,2-dihydro-indazol-3-one may exhibit unique properties and reactivity due to its specific substitution pattern, making it a subject of interest for researchers in organic chemistry and drug development.

4454-32-4

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4454-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4454-32-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,5 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4454-32:
(6*4)+(5*4)+(4*5)+(3*4)+(2*3)+(1*2)=84
84 % 10 = 4
So 4454-32-4 is a valid CAS Registry Number.

4454-32-4SDS

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 1-benzyl-2-methyl-1,2-dihydro-indazol-3-one

1.2 Other means of identification

Product number -
Other names 1-Benzyl-2-methyl-1,2-dihydro-indazol-3-on

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

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More Details:4454-32-4 SDS

4454-32-4Relevant academic research and scientific papers

Indazolinones, a new series of redox-active 5-lipoxygenase inhibitors with built-in selectivity and oral activity

Bruneau,Delvare,Edwards,McMillan

, p. 1028 - 1036 (1991)

Since the hypothetical mechanisms of hydroperoxydation of arachidonic acid by, respectively, 5-lipoxygenase (5-LPO) and cyclooxygenase (CO) involve a redox cycle, a compound which reduces 5-LPO and CO to their inactive state would give a nonselective inhi

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