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6-ethyl-5H-pyrrolo[3,4-b]pyridin-7(6H)-one is a heterocyclic organic compound characterized by a pyrrolo[3,4-b]pyridine core structure, which features a pyrrole ring fused to a pyridine ring. The compound has a 6-ethyl substituent, indicating an ethyl group attached to the sixth carbon atom of the pyrrolo[3,4-b]pyridine framework. This specific arrangement of atoms and functional groups endows the molecule with unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science. The compound's structure and properties make it a subject of interest for researchers exploring new chemical entities with specific biological activities or material properties.

1046121-01-0

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1046121-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1046121-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,1,2 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1046121-01:
(9*1)+(8*0)+(7*4)+(6*6)+(5*1)+(4*2)+(3*1)+(2*0)+(1*1)=90
90 % 10 = 0
So 1046121-01-0 is a valid CAS Registry Number.

1046121-01-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-ethyl-5H-pyrrolo[3,4-b]pyridin-7(6H)-one

1.2 Other means of identification

Product number -
Other names 6-ethyl-5,6-dihydro-7H-Pyrrolo[3,4-b]pyridin-7-one

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:1046121-01-0 SDS

1046121-01-0Downstream Products

1046121-01-0Relevant academic research and scientific papers

Novel synthesis of aza-phthalimidine hydroxylactams

Fan, Bolin,Liu, Zenglu,Tang, Mei,Xu, Yun,Tang, Xiaowei,Mao, Zhenmin

, p. 3231 - 3242 (2008/12/23)

A novel and convenient synthetic route for preparing aza-phthalimidine hydroxylactams (5a-j) by N-bromosuccinimide (NBS) was developed. This method involved the substitution reactions of substrates (3a-j) with NBS via unstable intermediate bromides (4a-j) rapidly hydrolyzed into hydroxyl products in the course of the workup process. Copyright Taylor & Francis Group, LLC.

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