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CAS

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742699-02-1

N-(2-bromobenzyl)-2-iodo-N-((trimethylsilyl)ethynyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 742699-02-1 Structure

  • Basic information

    1. Product Name: N-(2-bromobenzyl)-2-iodo-N-((trimethylsilyl)ethynyl)benzamide
    2. Synonyms: N-(2-bromobenzyl)-2-iodo-N-((trimethylsilyl)ethynyl)benzamide
    3. CAS NO:742699-02-1
    4. Molecular Formula:
    5. Molecular Weight: 512.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 742699-02-1.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: N-(2-bromobenzyl)-2-iodo-N-((trimethylsilyl)ethynyl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-bromobenzyl)-2-iodo-N-((trimethylsilyl)ethynyl)benzamide(742699-02-1)
    11. EPA Substance Registry System: N-(2-bromobenzyl)-2-iodo-N-((trimethylsilyl)ethynyl)benzamide(742699-02-1)

  • 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: 742699-02-1(Hazardous Substances Data)

742699-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 742699-02-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,2,6,9 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 742699-02:
(8*7)+(7*4)+(6*2)+(5*6)+(4*9)+(3*9)+(2*0)+(1*2)=191
191 % 10 = 1
So 742699-02-1 is a valid CAS Registry Number.

742699-02-1Relevant articles and documents

Synthesis of 3-(arylmethylene)isoindolin-1-ones from ynamides by Heck-Suzuki-Miyaura domino reactions. Application to the synthesis of lennoxamine

Couty, Sylvain,Liegault, Beno?t,Meyer, Christophe,Cossy, Janine

, p. 3882 - 3895 (2007/10/03)

Substituted 3-(arylmethylene)isoindolin-1-ones can be efficiently synthesized from various ynamides and boronic acids by palladium-catalyzed Heck-Suzuki-Miyaura domino reactions. This methodology has been applied to the total synthesis of lennoxamine and a concise route to this isoindolobenzazepine alkaloid was achieved in eight steps from 2,3-dimethoxybenzoic acid via a key intermediate ynamide.

Heck - Suzuki - Miyaura domino reactions involving ynamides. An efficient access to 3-(arylmethylene)isoindolinones

Couty, Sylvain,Liegault, Benoit,Meyer, Christophe,Cossy, Janine

, p. 2511 - 2514 (2007/10/03)

(Matrix Presented) Substituted 3-(arylmethylene)isoindolin-1-ones can be efficiently synthesized in a stereoselective manner from various ynamides and boronic acids by palladium-catalyzed Heck-Suzuki-Miyaura domino reactions.

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