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1186509-61-4

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1186509-61-4 Usage

Class

Indazole derivatives

Application

Research and pharmaceutical applications

Physical state

Yellow solid

Odor

Characteristic aromatic

Biological activities

Potential biological activities

Use

Precursor in the synthesis of various pharmaceutical compounds

Chemical structure

Unique chemical structure

Tool for studying

Biological and pharmacological properties of indazole derivatives

Developing

New drug candidates

Versatility

Potential applications in various fields including medicine and research

Check Digit Verification of cas no

The CAS Registry Mumber 1186509-61-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,6,5,0 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1186509-61:
(9*1)+(8*1)+(7*8)+(6*6)+(5*5)+(4*0)+(3*9)+(2*6)+(1*1)=174
174 % 10 = 4
So 1186509-61-4 is a valid CAS Registry Number.

1186509-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-1H-indazol-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1-benzyl-3-formylindazole

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:1186509-61-4 SDS

1186509-61-4Relevant articles and documents

Bis(dibenzylideneacetone)palladium(0)/tert-Butyl Nitrite- Catalyzed Cyclization of o-Alkynylanilines with tert-Butyl Nitrite: Synthesis and Applications of Indazole 2-Oxides

Senadi, Gopal Chandru,Wang, Ji-Qi,Gore, Babasaheb Sopan,Wang, Jeh-Jeng

, p. 2747 - 2753 (2017/08/23)

An efficient method for the synthesis of 1-benzyl/arylindazole 2-oxides via a bis(dibenzylideneacetone)palladium(0) [Pd(dba)2]/tert-butyl nitrite (TBN)-catalyzed reaction of o-alkynylaniline derivatives with TBN is reported. The overall transfo

PROCESS FOR THE PREPARATION OF 1-BENZYL-3-HYDR0XYMETHYL-1H-INDAZ0LE AND ITS DERIVATIVES AND REQUIRED MAGNESIUM INTERMEDIATES

-

Page/Page column 25; 26, (2011/02/24)

The present invention relates to the process for the preparation of 1-benzyl-3-hydroxymethyl-1H-indazole according to formula (II), to be used in a subsequent process for the preparation of 1-benzyl-3- hydroxymethyl-1H-indazole according to formula (I).

Efficient two-step sequence for the synthesis of 2,5-disubstituted furan derivatives from functionalized nitroalkanes: Successive Amberlyst A21- and Amberlyst 15-catalyzed processes

Palmieri, Alessandro,Gabrielli, Serena,Ballini, Roberto

supporting information; experimental part, p. 6165 - 6167 (2010/10/20)

The nitroaldol reaction of ketal-functionalized nitroalkanes with α-oxoaldehydes, promoted by Amberlyst A21, followed by acidic treatment (Amberlyst 15) of the obtained nitroalkanol, leads to the formation of 2,5-disubstituted furans in good yields. The p

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