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1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI) is a chemical compound that belongs to the pyrrolopyridine group. It is characterized by a heterocyclic structure with a pyrrolopyridine ring and a carboxaldehyde functional group, which makes it a versatile building block for the preparation of various complex molecules. Its unique structure and reactivity contribute to its value as a tool in the development of new chemical entities for a range of applications, including drug discovery and agricultural chemistry.

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  • 130473-26-6 Structure
  • Basic information

    1. Product Name: 1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI)
    2. Synonyms: 1H-Pyrrolo[2,3-C]pyridine-5-carbaldehyde;1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde;1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI)
    3. CAS NO:130473-26-6
    4. Molecular Formula: C8H6N2O
    5. Molecular Weight: 146.14604
    6. EINECS: N/A
    7. Product Categories: ALDEHYDE;PYRIDINE
    8. Mol File: 130473-26-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 353.864 °C at 760 mmHg
    3. Flash Point: 171.762 °C
    4. Appearance: /
    5. Density: 1.369 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 13.80±0.40(Predicted)
    10. CAS DataBase Reference: 1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI)(130473-26-6)
    12. EPA Substance Registry System: 1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI)(130473-26-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 130473-26-6(Hazardous Substances Data)

130473-26-6 Usage

Uses

Used in Organic Synthesis:
1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI) is used as a key intermediate in organic synthesis for the creation of complex organic molecules. Its reactivity and structural features facilitate the synthesis of a variety of compounds with potential applications in different fields.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI) is utilized as a building block for the development of pharmaceutical drugs. Its unique structure allows for the design of novel drug candidates with potential therapeutic properties.
Used in Drug Discovery:
1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI) is employed as a starting material in drug discovery processes. Its ability to form diverse chemical entities makes it a valuable component in the search for new and effective medications.
Used in Agrochemicals:
In agricultural chemistry, 1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI) is used as a component in the development of agrochemicals. Its versatility in forming complex molecules contributes to the creation of new compounds with potential applications in crop protection and enhancement of agricultural productivity.
Used in Chemical Research:
1H-Pyrrolo[2,3-c]pyridine-5-carboxaldehyde (9CI) is also used in chemical research to explore its properties and potential reactions, contributing to the advancement of knowledge in organic and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 130473-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,7 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130473-26:
(8*1)+(7*3)+(6*0)+(5*4)+(4*7)+(3*3)+(2*2)+(1*6)=96
96 % 10 = 6
So 130473-26-6 is a valid CAS Registry Number.

130473-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrrolo[2,3-c]pyridine-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1H-Pyrrolo<2,3-c>pyridine-5-carboxaldehyde

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:130473-26-6 SDS

130473-26-6Relevant articles and documents

Discovery of N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]furo[2,3-c]pyridine-5- carboxamide, an agonist of the α7 nicotinic acetylcholine receptor, for the potential treatment of cognitive deficits in schizophrenia: Synthesis and structure-activity relationship

Wishka, Donn G.,Walker, Daniel P.,Yates, Karen M.,Reitz, Steven C.,Jia, Shaojuan,Myers, Jason K.,Olson, Kirk L.,Jacobsen, E. Jon,Wolfe, Mark L.,Groppi, Vincent E.,Hanchar, Alexander J.,Thornburgh, Bruce A.,Cortes-Burgos, Luz A.,Wong, Erik H. F.,Staton, Brian A.,Raub, Thomas J.,Higdon, Nicole R.,Wall, Theron M.,Hurst, Raymond S.,Walters, Rodney R.,Hoffmann, William E.,Hajos, Mihaly,Franklin, Stanley,Carey, Galen,Gold, Lisa H.,Cook, Karen K.,Sands, Steven B.,Zhao, Sabrina X.,Soglia, John R.,Kalgutkar, Amit S.,Arneric, Stephen P.,Rogers, Bruce N.

, p. 4425 - 4436 (2007/10/03)

N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]furo[2,3-c]pyridine-5-carboxamide (14, PHA-543,613), a novel agonist of the α7 neuronal nicotinic acetylcholine receptor (α7 nAChR), has been identified as a potential treatment of cognitive deficits in schizophrenia. Compound 14 is a potent and selective a7 nAChR agonist with an excellent in vitro profile. The compound is characterized by rapid brain penetration and high oral bioavailability in rat and demonstrates in vivo efficacy in auditory sensory gating and, in an in vivo model to assess cognitive performance, novel object recognition.

COMPOUNDS HAVING BOTH α7 NICOTINIC AGONIST ACTIVITY AND 5HT3 ANTAGONIST ACTIVITY FOR TREATMENT OF CNS DISEASES

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Page 58, (2010/02/06)

The invention discloses compounds that are selective α7 nAChR agonists and 5-HT3 antagonists. The compounds are useful for treating many CNS diseases.

Azabicyclic-substituted fused-heteroaryl compounds for the treatment of disease

-

, (2008/06/13)

The invention provides compounds of Formula I: wherein Azabicyclo is These compounds may be in the form of pharmaceutical salts or compositions, racemic mixtures, or pure enantiomers thereof. The compounds of Formula I are useful in pharmaceuticals in which α7 is known to be involved.

Quinuclidines-substituted-multi-cyclic-heteroaryls for the treatment of disease

-

, (2008/06/13)

The invention provides compounds of Formula I: 1where in W is 2These compounds may be in the form of pharmaceutical salts or compositions, racemic mixtures, or pure enantiomers thereof. The compounds of Formula I are useful to treat diseases or conditions in which α7 is known to be involved.

Substituted 7-aza[2.2.1]bicycloheptanes for the treatment of disease

-

, (2008/06/13)

The invention provides compounds of Formula I: which may be in the form of pharmaceutical acceptable salts or compositions, are useful in treating diseases or conditions in which α7 nicotinic acetylcholine receptors (nAChRs) are known to be involved.

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