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CAS

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5-Methoxy-6-azaindole is an organic compound with the molecular formula C9H9N2O. It is a derivative of indole, featuring a methoxy group at the 5th position and an additional nitrogen atom at the 6th position, which distinguishes it as an azaindole. 5-Methoxy-6-azaindole is known for its potential applications in the pharmaceutical and chemical industries due to its unique structural properties.

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  • 17288-53-8 Structure
  • Basic information

    1. Product Name: 5-METHOXY-6-AZAINDOLE
    2. Synonyms: 5-METHOXY-6-AZAINDOLE;5-Methoxy-1H-pyrrolo[2,3-c]pyridine;5-Methxy-6-azaindole;1H-Pyrrolo[2,3-c]pyridine, 5-Methoxy-;5-Metho×y-1H-pyrrolo[2,3-c]pyridine;5-Methyl-1H-pyrrolo[2,3-c]pyridine;5-Methoxy-6-azaindole 96%
    3. CAS NO:17288-53-8
    4. Molecular Formula: C8H8N2O
    5. Molecular Weight: 148.16192
    6. EINECS: N/A
    7. Product Categories: Azaindoles;Building Blocks;C7 to C9;Chemical Synthesis;Heterocyclic Building Blocks;Indoles;Heterocycle-Pyridine series
    8. Mol File: 17288-53-8.mol
  • Chemical Properties

    1. Melting Point: 122-127 °C
    2. Boiling Point: 304℃
    3. Flash Point: 105℃
    4. Appearance: /
    5. Density: 1.244
    6. Vapor Pressure: 0.0016mmHg at 25°C
    7. Refractive Index: 1.647
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: 14.36±0.40(Predicted)
    11. CAS DataBase Reference: 5-METHOXY-6-AZAINDOLE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 5-METHOXY-6-AZAINDOLE(17288-53-8)
    13. EPA Substance Registry System: 5-METHOXY-6-AZAINDOLE(17288-53-8)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 17288-53-8(Hazardous Substances Data)

17288-53-8 Usage

Uses

Used in Pharmaceutical Industry:
5-Methoxy-6-azaindole is used as a reactant for the preparation of indole sulfonamides, which serve as HIV entry inhibitors. These compounds play a crucial role in the development of medications aimed at preventing the human immunodeficiency virus (HIV) from entering host cells, thus helping to combat the spread of the virus.
5-Methoxy-6-azaindole is also used as a reactant for the synthesis of melatoninergic ligands, including those with an azaindole moiety. Melatoninergic ligands are compounds that interact with melatonin receptors, which are involved in the regulation of sleep-wake cycles, mood, and other physiological processes. The development of such ligands can lead to the creation of novel treatments for various sleep disorders, mood disorders, and other conditions related to the melatonin system.

Check Digit Verification of cas no

The CAS Registry Mumber 17288-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,8 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17288-53:
(7*1)+(6*7)+(5*2)+(4*8)+(3*8)+(2*5)+(1*3)=128
128 % 10 = 8
So 17288-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O/c1-11-8-4-6-2-3-9-7(6)5-10-8/h2-5,9H,1H3

17288-53-8 Well-known Company Product Price

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  • Aldrich

  • (696463)  5-Methoxy-6-azaindole  96%

  • 17288-53-8

  • 696463-1G

  • 1,297.53CNY

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17288-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methoxy-1H-pyrrolo[2,3-c]pyridine

1.2 Other means of identification

Product number -
Other names 5-Methyl-1H-pyrrolo[2,3-c]pyridine

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:17288-53-8 SDS

17288-53-8Relevant articles and documents

ISOTOPICALLY LABELED BIARYL UREA COMPOUNDS

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Page/Page column 14; 15, (2014/01/07)

The present invention is directed to isotopically labeled biaryl urea compounds which possess high affinity to neurofibrillary tangles (NFTs), and thus are useful to determine the amount and distribution of NFTs in brain. The isotopically labeled biaryl urea compounds may also be useful as PET tracers and in competition assays to identify other compounds that may serve as PET tracers.

Pharmaceutically active 3-(1,2,5,6-tetrahydropyridyl)-pyrrolopyridines

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, (2008/06/13)

Compounds of the formula STR1 wherein one of A, B, D and E is N and the remaining three atoms are C; R1 and R2 are independently selected from hydrogen and C1 to C6 alkyl; and R3, R4, R5 and R6 are independently selected from hydrogen, halogen, hydroxy, C1 -C6 alkyl, C1 -C8 alkoxy, phenyl-C1 -C6 alkoxy, phenoxy --NR7 R8 wherein R7 and R8 are independently selected from hydrogen, C1 -C8 alkyl, C1 -C6 alkanoyl and COOR9 wherein R9 is hydrogen or C1 -C6 alkyl, cyano, COOR10 wherein R10 is hydrogen or C1 -C6 alkyl, and CONR11 R12 where R10 and R11 are independently selected from hydrogen and C1 -C6 alkyl, and the pharmaceutically acceptable salts thereof. The compounds are useful psychotherapeutics and may be used in treating obesity, depression and disorders wherein aggression is a symptom.

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