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1H-Pyrrolo[3,2-b]pyridine, 2,3-dihydrois a bicyclic heteroaromatic compound with a molecular formula C9H8N2. It features a pyrrolopyridine ring system and is utilized in medicinal chemistry and pharmaceutical research as a key building block for the synthesis of biologically active molecules. 1H-Pyrrolo[3,2-b]pyridine, 2,3-dihydrohas demonstrated promising properties in preclinical studies and has potential applications in the development of new drugs and as a fluorescent probe in analytical chemistry and bioimaging.

1211540-79-2

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1211540-79-2 Usage

Uses

Used in Pharmaceutical Research and Medicinal Chemistry:
1H-Pyrrolo[3,2-b]pyridine, 2,3-dihydrois used as a building block for the synthesis of various biologically active molecules, contributing to the development of new drugs. Its unique structure and properties make it a valuable component in the creation of pharmaceutical compounds with potential therapeutic applications.
Used in Analytical Chemistry and Bioimaging:
1H-Pyrrolo[3,2-b]pyridine, 2,3-dihydrois used as a fluorescent probe in analytical chemistry and bioimaging. Its fluorescent properties allow for the detection and visualization of specific biological processes or molecules, aiding in research and diagnostic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1211540-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,1,5,4 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1211540-79:
(9*1)+(8*2)+(7*1)+(6*1)+(5*5)+(4*4)+(3*0)+(2*7)+(1*9)=102
102 % 10 = 2
So 1211540-79-2 is a valid CAS Registry Number.

1211540-79-2SDS

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 2,3-dihydro-1H-pyrrolo[3,2-b]pyridine

1.2 Other means of identification

Product number -
Other names -

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:1211540-79-2 SDS

1211540-79-2Relevant academic research and scientific papers

NOVEL SUBSTITUTED TETRAHYDROQUINOLIN COMPOUNDS AS INDOLEAMINE 2,3-DIOXYGENASE (IDO) INHIBITORS

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, (2019/05/22)

Disclosed herein is a compound of formula (I), or a pharmaceutically acceptable salt thereof (I). Also disclosed herein are uses of the compounds disclosed herein in the potential treatment or prevention of an IDO-associated disease or disorder. Also disclosed herein are compositions comprising a compound disclosed herein. Further disclosed herein are uses of the compositions in the potential treatment or prevention of an IDO-associated disease or disorder.

CANCER TREATMENTS TARGETING CANCER STEM CELLS

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, (2019/11/19)

Disclosed are compounds, methods, compositions, and kits that allow for treating cancer by, e.g., targeting cancer stem cells. In some embodiments, the cancer is colorectal cancer, gastric cancer, gastrointestinal stromal tumor, ovarian cancer, lung cancer, breast cancer, pancreatic cancer, prostate cancer, testicular cancer, or lymphoma. In some embodiments, the cancer is liver cancer, endometrial cancer, leukemia, or multiple myeloma. The compounds utilized in the disclosure are of Formula (0), (O'), and (I):

This new pharmaceutical use (6-1, 6-dihydro-2-yl) amide derivative, as the inhibitor of this preparation and AKT (PKB) phosphoenzyme

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Paragraph 0466-0469, (2016/10/08)

The invention relates to the novel materials of formula (I), wherein each of the substituents R, R1, R2, R3, R4 and R5 is as defined herein. The materials are useful as inhibitors of AKT(PKB) phosphorylation.

INHIBITORS OF CYTOMEGALOVIRUS

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Page/Page column 89, (2014/05/24)

Compounds of Formula (I) wherein R1, R2, R3A, R3B, Y, Z1 and Z2 are defined herein, are useful for the treatment of cytomegalovirus disease and/or infection.

Preparation of azaindolines and benzoyl substituted azaindolines: Precursors of triazabenzo[cd]azulen-9-one PDE4 inhibitors

Badland, Matthew,Devillers, Ingrid,Durand, Corinne,Fasquelle, Véronique,Gaudillire, Bernard,Jacobelli, Henry,Manage, Ajith C.,Pevet, Isabelle,Puaud, Jocelyne,Shorter, Anthony J.,Wrigglesworth, Roger

, p. 5292 - 5296 (2011/10/30)

The syntheses of various substituted azaindolines are described. Azaindolines were identified as potential key intermediates towards new PDE4 inhibitors.

NEW COMPOUNDS, PHARMACEUTICAL COMPOSITION AND METHODS RELATING THERETO

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Page/Page column 32, (2011/01/12)

New compounds are disclosed which have utility in the treatment of a variety of metabolic related conditions in a patient. The compounds of this invention have the structure (I): wherein X1, X2, X3, X4, Y1

GPR 119 MODULATORS

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Page/Page column 59, (2010/11/18)

Compounds of Formula (I) that modulate the activity of the G -protein-coupled receptor GPFM 19 and their uses in the treatment of diseases linked to the modulation of the G-protein-coupled receptor GPR119 in animals are described herein.

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