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220904-92-7

5-(AMINOMETHYL)-1,3-DIHYDRO-2H-INDOL-2-ONE is a white crystalline solid with a molecular formula C9H10N2O and a molecular weight of 162.19 g/mol. It belongs to the indole class of chemical compounds and has potential biological and pharmacological activities. The presence of the amino and carbonyl group in its structure makes it a versatile compound for use in organic synthesis and drug development. However, it is important to handle this chemical with caution due to its potential reactivity and toxicological properties.

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  • 220904-92-7 Structure

  • Basic information

    1. Product Name: 5-(AMINOMETHYL)-1,3-DIHYDRO-2H-INDOL-2-ONE
    2. Synonyms: 5-(AMINOMETHYL)-1,3-DIHYDRO-2H-INDOL-2-ONE;5-(aminomethyl)indolin-2-one;2H-Indol-2-one, 5-(aMinoMethyl)-1,3-dihydro-;5-AMinoMethyl-1,3-dihydro-indol-2-one
    3. CAS NO:220904-92-7
    4. Molecular Formula: C9H10N2O
    5. Molecular Weight: 162.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 220904-92-7.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.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-(AMINOMETHYL)-1,3-DIHYDRO-2H-INDOL-2-ONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(AMINOMETHYL)-1,3-DIHYDRO-2H-INDOL-2-ONE(220904-92-7)
    11. EPA Substance Registry System: 5-(AMINOMETHYL)-1,3-DIHYDRO-2H-INDOL-2-ONE(220904-92-7)

  • 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: 220904-92-7(Hazardous Substances Data)

220904-92-7 Usage

Uses

Used in Pharmaceutical Industry:
5-(AMINOMETHYL)-1,3-DIHYDRO-2H-INDOL-2-ONE is used as a pharmaceutical candidate for its potential medicinal applications. Its unique structure and properties make it a promising compound for the development of new drugs and therapies.
Used in Organic Synthesis:
5-(AMINOMETHYL)-1,3-DIHYDRO-2H-INDOL-2-ONE is used as a versatile compound in organic synthesis. Its amino and carbonyl groups allow for various chemical reactions and modifications, making it a valuable building block for the synthesis of more complex molecules.
Used in Drug Development:
5-(AMINOMETHYL)-1,3-DIHYDRO-2H-INDOL-2-ONE is used in drug development for its potential to be incorporated into new drug formulations. Its unique properties and reactivity make it a promising candidate for the development of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 220904-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,9,0 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 220904-92:
(8*2)+(7*2)+(6*0)+(5*9)+(4*0)+(3*4)+(2*9)+(1*2)=107
107 % 10 = 7
So 220904-92-7 is a valid CAS Registry Number.

220904-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(aminomethyl)-1,3-dihydroindol-2-one

1.2 Other means of identification

Product number -
Other names 5-(aminomethyl)-1,3-dihydro-2H-indol-2-one

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:220904-92-7 SDS

220904-92-7Downstream Products

220904-92-7Relevant articles and documents

Benzylidene-1,3-dihydro-indol-2-one derivatives a receptor tyrosine kinase inhibitors, particularly of Raf kinases

-

, (2008/06/13)

Compounds of general formula (I) wherein: R1is H or optionally joined with R2to form a fused ring selected from the group consisting of five to ten membered aryl, heteroaryl or heterocyclyl rings, R2and R3are in

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