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754214-46-5

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754214-46-5 Usage

Molecular structure

A compound with a pyrrolopyridine core and a carboxaldehyde functional group.

T-butyl and dimethylsilyl groups

Enhance the stability and reactivity of the compound.

Potential applications

Organic synthesis, medicinal chemistry, and material science.

Versatile reactivity

Allows for the development of new compounds and materials.

Structural features

Unique properties making it a valuable building block in chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 754214-46-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,4,2,1 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 754214-46:
(8*7)+(7*5)+(6*4)+(5*2)+(4*1)+(3*4)+(2*4)+(1*6)=155
155 % 10 = 5
So 754214-46-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2OSi/c1-14(2,3)18(4,5)16-7-6-12-8-11(10-17)9-15-13(12)16/h6-10H,1-5H3

754214-46-5SDS

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 1H-Pyrrolo[2,3-b]pyridine-5-carboxaldehyde, 1-[(1,1-dimethylethyl)dimethylsilyl]-

1.2 Other means of identification

Product number -
Other names 2-PROPANOL,1-[[(1,1-DIMETHYLETHYL)DIMETHYLSILYL]OXY]-,(2S)

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:754214-46-5 SDS

754214-46-5Relevant articles and documents

SYNTHESIS

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Page 55; 57, (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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