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136888-26-1

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136888-26-1 Usage

General Description

5,6-dichloro-1H-pyrrolo[3,2-b]pyridin-2(3H)-one is a chemical compound with the molecular formula C7H3Cl2N2O. It is a heterocyclic compound that consists of a pyrrolopyridine ring fused to a pyrazin-2(3H)-one. 5,6-dichloro-1H-pyrrolo[3,2-b]pyridin-2(3H)-one is a chlorinated derivative of the parent compound, pyrrolo[3,2-b]pyridin-2(3H)-one. It has potential applications in pharmaceuticals and agrochemicals due to its unique structure and properties. 5,6-dichloro-1H-pyrrolo[3,2-b]pyridin-2(3H)-one is of interest to researchers and industry professionals for its potential as a starting material for the synthesis of novel bioactive molecules. Its precise applications and properties are still being studied and explored.

Check Digit Verification of cas no

The CAS Registry Mumber 136888-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,8 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136888-26:
(8*1)+(7*3)+(6*6)+(5*8)+(4*8)+(3*8)+(2*2)+(1*6)=171
171 % 10 = 1
So 136888-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H4Cl2N2O/c8-3-1-4-5(11-7(3)9)2-6(12)10-4/h1H,2H2,(H,10,12)

136888-26-1SDS

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 5,6-Dichloro-1H-pyrrolo[3,2-b]pyridin-2(3H)-one

1.2 Other means of identification

Product number -
Other names 5,6-dichloro-1,3-dihydropyrrolo[3,2-b]pyridin-2-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:136888-26-1 SDS

136888-26-1Downstream Products

136888-26-1Relevant articles and documents

AZAINDOLE DERIVATIVE HAVING AMPK-ACTIVATING EFFECT

-

Paragraph 0172; 0174; 0181; 0182, (2017/07/14)

Disclosed is a compound which is useful as an AMPK activator. A compound represented by formula: or its pharmaceutically acceptable salt, wherein X is substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, or substituted or unsubstituted heterocyclyl; R1 is hydrogen, halogen, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted acyl, substituted or unsubstituted carbamoyl, substituted or unsubstituted alkylthio, substituted or unsubstituted alkylsulfinyl, substituted or unsubstituted alkylsulfonyl, or substituted or unsubstituted alkyloxycarbonyl; R2 is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted heterocyclyl, or the like; R3 is halogen, hydroxy, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkenyl, substituted or unsubstituted heterocyclyl, or the like; and R4 is hydrogen, halogen, hydroxy, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, or the like.

Synthesis of substituted azaoxindoles for the preparation of aza-tenidap analogs

Robinson, Ralph P.,Donahue, Kathleen M.,Son, Paul S.,Wagy, Steven D.

, p. 287 - 293 (2007/10/03)

The preparation of a set of eight azaoxindoles bearing substituents on the aromatic nucleus is outlined. These compounds were required for the preparation of aza-analogs of the anti-inflammatory oxindole tenidap. Two methods of synthesis were used, the fi

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