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611204-94-5

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611204-94-5 Usage

Structure

Pyrrolo[2,3-b]pyridine with a 2-thienyl substitution
Contains both pyridine and pyrrole rings, with a thiophene group attached to the 5-position of the pyrrolopyridine core.
3. Heterocyclic compound
A compound containing one or more rings with atoms of different elements, in this case, carbon, nitrogen, and sulfur.
4. Biological activities
Exhibits diverse biological activities, such as anti-cancer and anti-inflammatory properties.
5. Potential applications
Has potential use in pharmaceuticals and agrochemicals due to its various biological activities.
6. Importance in medicinal chemistry
The unique structure and properties make it a promising candidate for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 611204-94-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,1,2,0 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 611204-94:
(8*6)+(7*1)+(6*1)+(5*2)+(4*0)+(3*4)+(2*9)+(1*4)=105
105 % 10 = 5
So 611204-94-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H8N2S/c1-2-10(14-5-1)9-6-8-3-4-12-11(8)13-7-9/h1-7H,(H,12,13)

611204-94-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2-methyl-1H-indol-4-yl)oxy]-3-piperidin-1-ylpropan-2-ol

1.2 Other means of identification

Product number -
Other names 1-(2-Methyl-1H-indol-4-yloxy)-3-piperidin-1-yl-propan-2-ol

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:611204-94-5 SDS

611204-94-5Downstream Products

611204-94-5Relevant articles and documents

SYNTHESIS

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Page 69-70, (2010/02/08)

The present invention provides a novel substituted azaindoline intermediate of formula (I) and a method for its synthesis. The novel substitued azaindoline intermediate (I) is provided for use in the manufacture of 5-substituted 7-azaindolines and 5-substituted 7-azaindoles.

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