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100394-77-2

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100394-77-2 Usage

Derivative of indazole

A class of heterocyclic organic compounds

Contains a nitro group

A functional group consisting of an oxygen atom double-bonded to a nitrogen atom (-NO2)

Contains a phenyl group

A functional group consisting of a six-membered carbon ring with alternating single and double bonds (C6H5)

Attached to the indazole ring

The phenyl and nitro groups are connected to the five-membered indazole ring

Used in pharmaceutical research and drug development

It is being studied for its potential applications in the treatment of various conditions

Potential applications in the treatment of various conditions

The specific conditions it may be useful in treating are not specified in the provided material

Interesting for studying its biological activity

The compound's structure and properties make it a good candidate for further research into how it interacts with biological systems

Potential therapeutic uses

The specific therapeutic uses of the compound are not specified in the provided material, but its structure and properties suggest it may have potential in this area.

Check Digit Verification of cas no

The CAS Registry Mumber 100394-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,9 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100394-77:
(8*1)+(7*0)+(6*0)+(5*3)+(4*9)+(3*4)+(2*7)+(1*7)=92
92 % 10 = 2
So 100394-77-2 is a valid CAS Registry Number.

100394-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-nitrophenyl)-4,5,6,7-tetrahydro-1H-indazole

1.2 Other means of identification

Product number -
Other names 1-(4-nitro-phenyl)-4,5,6,7-tetrahydro-1H-indazole

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:100394-77-2 SDS

100394-77-2Downstream Products

100394-77-2Relevant articles and documents

Palladium-catalyzed C-N bond formation: synthesis of 1-aryl-1H-pyrazoles from β-bromovinyl aldehydes and arylhydrazines

Cho, Chan Sik,Patel, Daksha B.

, p. 6388 - 6391 (2006)

Cyclic and acyclic β-bromovinyl aldehydes are cyclized with an array of arylhydrazines in toluene at 125 °C in the presence of a palladium catalyst and a phosphorus chelating ligand together with NaOtBu to give 1-aryl-1H-pyrazoles in moderate t

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