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1-methyl-6,7-dihydro-1H-indazol-4(5H)-one is a heterocyclic chemical compound characterized by its molecular formula C9H10N2O. It features an indazole ring fused with a dihydro structure and a ketone functional group. 1-methyl-6,7-dihydro-1H-indazol-4(5H)-one is notable for its potential applications in pharmaceutical research and drug development, stemming from its distinctive structural attributes and the biological activities it may exhibit. It also serves as a valuable building block in organic synthesis for creating a diverse array of compounds. Furthermore, it has been the subject of research for its possible pharmacological effects, indicating its utility in the development of novel therapeutic agents for a range of diseases and conditions.

85302-16-5

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85302-16-5 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
1-methyl-6,7-dihydro-1H-indazol-4(5H)-one is utilized as a key component in the design and synthesis of new pharmaceutical agents due to its unique molecular structure and potential to modulate biological targets. Its presence in drug candidates can contribute to desired pharmacological properties, such as selectivity and potency.
Used in Organic Synthesis:
As a building block in organic synthesis, 1-methyl-6,7-dihydro-1H-indazol-4(5H)-one is employed for the preparation of a variety of complex organic compounds. Its reactivity and structural features make it a versatile intermediate for the synthesis of target molecules in various chemical and pharmaceutical applications.
Used in the Development of New Therapeutics:
1-methyl-6,7-dihydro-1H-indazol-4(5H)-one is studied for its potential pharmacological effects, which may lead to its application in the development of innovative drugs for treating a spectrum of diseases and conditions. Its exploration in this context is driven by the need for new molecular entities that can address unmet medical needs and offer improved treatment options.

Check Digit Verification of cas no

The CAS Registry Mumber 85302-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,0 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85302-16:
(7*8)+(6*5)+(5*3)+(4*0)+(3*2)+(2*1)+(1*6)=115
115 % 10 = 5
So 85302-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O/c1-10-7-3-2-4-8(11)6(7)5-9-10/h5H,2-4H2,1H3

85302-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-6,7-dihydro-5H-indazol-4-one

1.2 Other means of identification

Product number -
Other names 1,5,6,7-tetrahydro-1-methyl-1H-indazol-4-one

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:85302-16-5 SDS

85302-16-5Relevant academic research and scientific papers

Reaction of 2-Dimethylaminomethylene-1,3-diones with Dinucleophiles. I. Synthesis of 1,5-Disubstituted 4-Acylpyrazoles

Schenone, Pietro,Mosti, Luisa,Menozzi, Giulia

, p. 1355 - 1361 (2007/10/02)

Reaction of open-chain and cyclic sym-1,3-diones with N,N-dimethylformamide dimethyl acetal gave, generally in high yield, a series of sym-2-dimethylaminomethylene-1,3-diones which reacted with phenylhydrazine and methylhydrazine to afford, generally in satisfactory yield, a number of 1,5-disubstituted 4-acylpyrazoles.The applications and limits of this new pyrazole synthesis are presented and discussed.

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