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2,5,6,7-Tetrahydro-2-methyl-4h-indazol-4-one is a heterocyclic chemical compound with the molecular formula C9H10N2O. It features a unique fused indazole ring system, which contributes to its potential applications in the pharmaceutical industry. 2,5,6,7-Tetrahydro-2-methyl-4h-indazol-4-one is of interest to scientists and researchers due to its promising structure and properties for the development of new drugs and therapeutic agents in the field of medicinal chemistry.

1027617-67-9

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1027617-67-9 Usage

Uses

Used in Pharmaceutical Industry:
2,5,6,7-Tetrahydro-2-methyl-4h-indazol-4-one is used as a key intermediate in the synthesis of various pharmaceutical compounds for the development of new drugs and therapeutic agents. Its unique chemical structure and properties make it a valuable candidate for further research and development in medicinal chemistry.
Used in Medicinal Chemistry Research:
2,5,6,7-Tetrahydro-2-methyl-4h-indazol-4-one serves as a promising scaffold for the design and synthesis of novel bioactive molecules with potential pharmacological activities. Researchers utilize 2,5,6,7-Tetrahydro-2-methyl-4h-indazol-4-one to explore its potential biological effects and develop new therapeutic agents for various diseases and medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1027617-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,6,1 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1027617-67:
(9*1)+(8*0)+(7*2)+(6*7)+(5*6)+(4*1)+(3*7)+(2*6)+(1*7)=139
139 % 10 = 9
So 1027617-67-9 is a valid CAS Registry Number.

1027617-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-6,7-dihydro-5H-indazol-4-one

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

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:1027617-67-9 SDS

1027617-67-9Downstream Products

1027617-67-9Relevant articles and documents

Design, synthesis and biological evaluation of selective histone deacetylase 6 (HDAC6) inhibitors bearing benzoindazole or pyrazoloindazole scaffold as surface recognition motif

Xu, Qihao,Mou, Yanhua,Wang, Siyuan,Gao, Xiaoxiao,Zhang, Yulong,Wang, Zhi,Xu, Xiangwei,Han, Yu,Jia, Wenlong,Zhang, Meihui,Zhao, Linxiang,Liu, Dan

, (2021)

A series of compounds were designed and synthesized based on the compound 11i bearing phenylpyrazole scaffold with histone deacetylase 6 (HDAC6) inhibitory activity. Most of the compounds showed considerable inhibitory activity against HDAC6 and compound

AMINOACYLINDAZOLE IMMUNOMODULATORS FOR TREATMENT OF AUTOIMMUNE DISEASES

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, (2017/12/29)

2-Acylindazole compounds of formula I or formula II are disclosed. These compounds inhibit Coagulation Factor XIIa. They are useful to treat autoimmune diseases.

AMINOPYRAZOLOQUINAZOLINES

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Page/Page column 20, (2012/09/25)

Compounds of general formula (I) wherein the groups R1 to R3 and X are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, pharmaceutical preparations whi

NEW AMINOPYRAZOLOQUINAZOLINES

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Page/Page column 51, (2012/02/05)

The present invention encompasses compounds of general formula (I) wherein the groups R1 to R3 and X are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferatio

An expedient synthesis of regioisomeric pyrazole-fused cycloalkanones

Kennedy, Lawrence J.

, p. 600 - 604 (2008/12/22)

Described herein is a novel one-pot procedure for the synthesis of pyrazoles through the in situ generation of a monohydrazone of cyclic 1,3-diones and subsequent cyclization with N,N-dimethylformamide dimethyl acetal. This route provides pyrazoles that have limited accessibility by other methods. Georg Thieme Verlag Stuttgart.

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