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1-benzyl-2,3-dihydro-1H-indol-6-amine is a heterocyclic chemical compound belonging to the group of indole derivatives. It features an indole ring with an amine group at the 6th position and a benzyl group attached to the nitrogen atom. 1-benzyl-2,3-dihydro-1H-indol-6-amine holds potential pharmaceutical importance due to its diverse biological activities.

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  • 256924-07-9 Structure
  • Basic information

    1. Product Name: 1-benzyl-2,3-dihydro-1H-indol-6-amine
    2. Synonyms: 1-benzyl-2,3-dihydro-1H-indol-6-amine;1h-indol-6-aMine,2,3-dihydro-1-(phenylMethyl)-;1-Benzylindolin-6-aMine;1-Benzyl-2,3-dihydro-1H-indol-6-ylamine
    3. CAS NO:256924-07-9
    4. Molecular Formula: C15H16N2
    5. Molecular Weight: 224.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 256924-07-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-benzyl-2,3-dihydro-1H-indol-6-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyl-2,3-dihydro-1H-indol-6-amine(256924-07-9)
    11. EPA Substance Registry System: 1-benzyl-2,3-dihydro-1H-indol-6-amine(256924-07-9)
  • 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: 256924-07-9(Hazardous Substances Data)

256924-07-9 Usage

Uses

Used in Pharmaceutical Industry:
1-benzyl-2,3-dihydro-1H-indol-6-amine is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and treatments.
1-benzyl-2,3-dihydro-1H-indol-6-amine is used as an intermediate in the synthesis of organic compounds, facilitating the creation of complex molecules for medicinal and therapeutic applications.
Used in Research and Development:
1-benzyl-2,3-dihydro-1H-indol-6-amine is utilized in research and development activities within the pharmaceutical and chemical industries, aiding in the discovery and understanding of its biological properties and potential applications in drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 256924-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,9,2 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 256924-07:
(8*2)+(7*5)+(6*6)+(5*9)+(4*2)+(3*4)+(2*0)+(1*7)=159
159 % 10 = 9
So 256924-07-9 is a valid CAS Registry Number.

256924-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-2,3-dihydroindol-6-amine

1.2 Other means of identification

Product number -
Other names 1H-Indol-6-amine,2,3-dihydro-1-(phenylmethyl)

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:256924-07-9 SDS

256924-07-9Relevant articles and documents

Novel squarylium compounds, resin composition for absorbing near infrared ray including the same and absorbing near infrared ray blocking filter manufactured by using this

-

, (2018/05/15)

The present invention refers to near infrared filter a squarylium compound, including near-infrared absorbing resin composition for same, a near-infrared cut filter and their use relates to search using the number bath, more specifically maximum absorption wavelength is 630 - 750 nm, light absorption coefficient and good solubility in the near-infrared cut filter mole for near-infrared absorbing processed a squarylium compound, near-infrared absorbing resin composition and by using a near-infrared cut filter to number tank are disclosed. (by machine translation)

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