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1038515-22-8

2-(3-methylbut-2-enyl)-1-tosyl-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1038515-22-8 Structure

  • Basic information

    1. Product Name: 2-(3-methylbut-2-enyl)-1-tosyl-1H-indole
    2. Synonyms: 2-(3-methylbut-2-enyl)-1-tosyl-1H-indole
    3. CAS NO:1038515-22-8
    4. Molecular Formula:
    5. Molecular Weight: 339.458
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1038515-22-8.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: 2-(3-methylbut-2-enyl)-1-tosyl-1H-indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3-methylbut-2-enyl)-1-tosyl-1H-indole(1038515-22-8)
    11. EPA Substance Registry System: 2-(3-methylbut-2-enyl)-1-tosyl-1H-indole(1038515-22-8)

  • 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: 1038515-22-8(Hazardous Substances Data)

1038515-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1038515-22-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,8,5,1 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1038515-22:
(9*1)+(8*0)+(7*3)+(6*8)+(5*5)+(4*1)+(3*5)+(2*2)+(1*2)=128
128 % 10 = 8
So 1038515-22-8 is a valid CAS Registry Number.

1038515-22-8Downstream Products

1038515-22-8Relevant articles and documents

Stable Bromiranium Ion Salts as Reagents for Biomimetic Indole Terpenoid Cyclizations

Bock, Jonathan,Daniliuc, Constantin G.,Hennecke, Ulrich

, p. 1704 - 1707 (2019)

Indole terpene alkaloids are a diverse group of natural products and show significant biological activities. To enable their biomimetic synthesis, electrophilic bromocyclization of polyenyl indole derivatives could be achieved using sterically demanding b

Synthesis of unsaturated tryprostatin B analogues and determination of their enantiomeric purity with (S)-1-benzyl-6-methylpiperazine-2,5-dione

Wagger, Jernej,Svete, Jurij,Stanovnik, Branko

, p. 1436 - 1442 (2008)

Novel racemic and enantiomerically enriched unsaturated tryprostatin B analogues were synthesised by an enaminone-based strategy. The synthesis also features a novel coppers-catalysed dipeptide formation. In addition, the enantiomeric purity of an enantio

Synthesis of racemic, n-benzylated neoechinulin a and isoneoechinulin A1

Wagger, Jernej,Groselj, Uros,Svete, Jurij,Stanovnik, Branko

scheme or table, p. 1197 - 1200 (2010/08/05)

Two N-benzylated analogues of the antioxidant, radical scavenging, and neUrosprotective alkaloid neoechinulin A were prepared. Since, according to SAR studies, stereochemistry does not play an important role, both analogues were prepared in racemic form, using enaminone chemistry. Georg Thieme Verlag Stuttgart.

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