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83948-32-7

4-amino-4-(3,4-dimethoxy-6-iodophenyl)-1-butene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83948-32-7 Structure

  • Basic information

    1. Product Name: 4-amino-4-(3,4-dimethoxy-6-iodophenyl)-1-butene
    2. Synonyms:
    3. CAS NO:83948-32-7
    4. Molecular Formula:
    5. Molecular Weight: 333.169
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83948-32-7.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: 4-amino-4-(3,4-dimethoxy-6-iodophenyl)-1-butene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-amino-4-(3,4-dimethoxy-6-iodophenyl)-1-butene(83948-32-7)
    11. EPA Substance Registry System: 4-amino-4-(3,4-dimethoxy-6-iodophenyl)-1-butene(83948-32-7)

  • 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: 83948-32-7(Hazardous Substances Data)

83948-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83948-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,4 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83948-32:
(7*8)+(6*3)+(5*9)+(4*4)+(3*8)+(2*3)+(1*2)=167
167 % 10 = 7
So 83948-32-7 is a valid CAS Registry Number.

83948-32-7Relevant articles and documents

Preparation of Primary Amines and 2-Azetidinones via N-Trimethylsilyl Imines

Hart, David J.,Kanai, Ken-ichi,Thomas, Dudley G.,Yang, Teng-Kuei

, p. 289 - 294 (2007/10/02)

Nonenolizable aldehydes react with lithium bis(trimethylsilyl)amide at ambient temperatures to afford solutions of N-trimethylsilyl aldimines.Treatment of these solutions with Grignard reagents or alkyllithiums followed by an aqueous workup gives primary amines in moderate to excellent yields.Treatment of N-trimethylsilyl aldimines with ester enolates provides an expedient route to 1-unsubstituted 2-azetidinones.

New Approach to Lythraceae Alkaloids: Total Synthesis of (+/-)-Vertaline

Hart, David J.,Kanai, Ken-ichi

, p. 1555 - 1560 (2007/10/02)

A new approach to Lythraceae alkaloids is described within the context of a total synthesis of (+/-)-vertaline (2).The use of N-silyl imines in the preparation of benzylic amines as well as a stereoselective bicycloannelation approach to the synthesis of quinolizidinones is discussed.

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