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26487-02-5

3-ethoxy-1-isoindolinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 26487-02-5 Structure

  • Basic information

    1. Product Name: 3-ethoxy-1-isoindolinone
    2. Synonyms: 3-ethoxy-1-isoindolinone
    3. CAS NO:26487-02-5
    4. Molecular Formula: C10H11NO2
    5. Molecular Weight: 177.19984
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26487-02-5.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: 3-ethoxy-1-isoindolinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-ethoxy-1-isoindolinone(26487-02-5)
    11. EPA Substance Registry System: 3-ethoxy-1-isoindolinone(26487-02-5)

  • 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: 26487-02-5(Hazardous Substances Data)

26487-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26487-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,8 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26487-02:
(7*2)+(6*6)+(5*4)+(4*8)+(3*7)+(2*0)+(1*2)=125
125 % 10 = 5
So 26487-02-5 is a valid CAS Registry Number.

26487-02-5Relevant articles and documents

One-pot synthesis of 3-alkoxy-2,3-dihydro-1H-isoindol-1-ones by the reactions of 2-(Azidomethyl)benzoates with NaH

Kobayashi, Kazuhiro,Chikazawa, Yuuki,Ezaki, Kosuke

, p. 604 - 610 (2015)

Abstract A new and facile method for the general preparation of 3-alkoxy-2,3-dihydro-1H-isoindol-1-ones has been developed. Thus, the reaction of 2-(azidomethyl)benzoates with NaH affords, after workup with H2O, 3-alkoxy-2,3-dihydro-1H-isoindol

A REMOVABLE AUXILIARY FOR AMIDOMERCURATION REACTIONS: THE STEREOCONTROLLED PREPARATION OF VICINAL AMINOALCOHOLS

Takacs, James M.,Helle, Mark A.,Yang, Linrong

, p. 1777 - 1780 (2007/10/02)

Unsaturated amidals 1, derived from allylic alcohols and containing a stereogenic amidal center, undergo amidomercuration with high 1,3-stereoinduction from the amidal center.In substrates derived from secondary allylic alcohols, the influence of the ster

Synthesis of Isoindoles. Acid or Base Induced Cyclization of 2-Cyanobenzaldehyde with Alcohols

Sato, Ryu,Ohmori, Michiko,Kaitani, Fumiko,Kurosawa, Akiko,Senzaki, Toshihide,et al.

, p. 2481 - 2486 (2007/10/02)

Various 3,3-dialkoxy-2,3-dihydro-1-hydroxy-1H-isoindoles (2) were obtained by treating 2-cyanobenzaldehyde (1) with alcohols in the presence of an acid catalyst such as silica gel.In the reaction using a base catalyst such as triethylamine and 1,8-diazabi

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