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CAS

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74492-44-7

1-benzyl-5-methoxyindoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74492-44-7 Structure

  • Basic information

    1. Product Name: 1-benzyl-5-methoxyindoline
    2. Synonyms: 1-benzyl-5-methoxyindoline
    3. CAS NO:74492-44-7
    4. Molecular Formula:
    5. Molecular Weight: 239.317
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74492-44-7.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: 1-benzyl-5-methoxyindoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyl-5-methoxyindoline(74492-44-7)
    11. EPA Substance Registry System: 1-benzyl-5-methoxyindoline(74492-44-7)

  • 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: 74492-44-7(Hazardous Substances Data)

74492-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74492-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,9 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74492-44:
(7*7)+(6*4)+(5*4)+(4*9)+(3*2)+(2*4)+(1*4)=147
147 % 10 = 7
So 74492-44-7 is a valid CAS Registry Number.

74492-44-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-5-methoxyindoline

1.2 Other means of identification

Product number -
Other names 5-methoxy-1-benzylindoline

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:74492-44-7 SDS

74492-44-7Relevant articles and documents

Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles

Maier, Alexander F. G.,Tussing, Sebastian,Schneider, Tobias,Fl?rke, Ulrich,Qu, Zheng -Wang,Grimme, Stefan,Paradies, Jan

, p. 12219 - 12223 (2016/10/13)

An acceptorless dehydrogenation of heterocycles catalyzed by frustrated Lewis pairs (FLPs) was developed. Oxidation with concomitant liberation of molecular hydrogen proceeded in high to excellent yields for N-protected indolines as well as four other substrate classes. The mechanism of this unprecedented FLP-catalyzed reaction was investigated by mechanistic studies, characterization of reaction intermediates by NMR spectroscopy and X-ray crystal analysis, and by quantum-mechanical calculations. Hydrogen liberation from the ammonium hydridoborate intermediate is the rate-determining step of the oxidation. The addition of a weaker Lewis acid as a hydride shuttle increased the reaction rate by a factor of 2.28 through a second catalytic cycle.

INDOLINE DERIVATIVES

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Page/Page column 16, (2011/12/13)

The present invention provides a novel indoline derivative or a pharmacologically acceptable salt thereof or a solvate of the derivative or a salt thereof represented by the following formula (1) that has an excellent butyrylcholinesterase inhibitory acti

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