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1036007-71-2

5-(Benzyloxy)-1H-pyrrolo[2,3-b]pyridine is a chemical compound with the molecular formula C13H11N3O. It is a derivative of pyrrolo[2,3-b]pyridine, featuring a benzyloxy group attached to the 5-position of the pyrrolo[2,3-b]pyridine core. 5-(Benzyloxy)-1h-pyrrolo[2,3-b]pyridine is of interest in medicinal chemistry, particularly in the development of potential therapeutic agents, due to its unique structure and the ability to form hydrogen bonds. It is synthesized through various chemical reactions and can be used as a building block for more complex molecules. The compound's properties, such as solubility and stability, can be influenced by the presence of the benzyloxy group, making it a valuable intermediate in the synthesis of pharmaceuticals and other bioactive molecules.

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  • 1036007-71-2 Structure

  • Basic information

    1. Product Name: 5-(Benzyloxy)-1h-pyrrolo[2,3-b]pyridine
    2. Synonyms: 5-Benzyloxy-1H-pyrrolo[2,3-b]pyridine
    3. CAS NO:1036007-71-2
    4. Molecular Formula: C14H12N2O
    5. Molecular Weight: 224.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036007-71-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-(Benzyloxy)-1h-pyrrolo[2,3-b]pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(Benzyloxy)-1h-pyrrolo[2,3-b]pyridine(1036007-71-2)
    11. EPA Substance Registry System: 5-(Benzyloxy)-1h-pyrrolo[2,3-b]pyridine(1036007-71-2)

  • 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: 1036007-71-2(Hazardous Substances Data)

1036007-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036007-71-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,0,0 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1036007-71:
(9*1)+(8*0)+(7*3)+(6*6)+(5*0)+(4*0)+(3*7)+(2*7)+(1*1)=102
102 % 10 = 2
So 1036007-71-2 is a valid CAS Registry Number.

1036007-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(benzyloxy)-1H-pyrrolo[2,3-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:1036007-71-2 SDS

1036007-71-2Downstream Products

1036007-71-2Relevant articles and documents

AROMATIC RING DERIVATIVE AS IMMUNOREGULATION AND PREPARATION METHOD AND APPLICATION OF AROMATIC RING DERIVATIVE

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Paragraph 0185-0186, (2021/10/15)

Relating to a compound represented by formula (I) and a pharmaceutically acceptable salt of the compound, and an application of the compound as an S1P1 agonist.

Preparation method 5- hydroxyl -7- azaindole (by machine translation)

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, (2020/04/06)

The invention discloses 5 -hydroxy- 7 7-azaindole preparation method, which takes 5 - X - 2 -nitropyridine as a raw material to react with benzyl alcohol sodium or sodium alkyl sodium alkoxide to generate 5 - R - 2 -nitropyridine, which is benzyl, methyl or ethyl X after being closed by a Grignard reagent ring after cyclization is carried, out, and ;R is high, yield. (by machine translation)

PYRROLO [2,3-B] PYRIDINES AS KINASE MODULATORS

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Page/Page column 66, (2008/12/07)

Compounds active on protein kinases are described, as well as methods of using such compounds to treat diseases and conditions associated with aberrant activity of protein kinases.

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