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1238861-80-7

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

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  • 1238861-80-7 Structure

  • Basic information

    1. Product Name: (E)-3-(2-(2-bromophenyl)ethenyl)-1(H)-indole
    2. Synonyms: (E)-3-(2-(2-bromophenyl)ethenyl)-1(H)-indole
    3. CAS NO:1238861-80-7
    4. Molecular Formula:
    5. Molecular Weight: 298.182
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1238861-80-7.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: (E)-3-(2-(2-bromophenyl)ethenyl)-1(H)-indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-3-(2-(2-bromophenyl)ethenyl)-1(H)-indole(1238861-80-7)
    11. EPA Substance Registry System: (E)-3-(2-(2-bromophenyl)ethenyl)-1(H)-indole(1238861-80-7)

  • 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: 1238861-80-7(Hazardous Substances Data)

1238861-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1238861-80-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,8,8,6 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1238861-80:
(9*1)+(8*2)+(7*3)+(6*8)+(5*8)+(4*6)+(3*1)+(2*8)+(1*0)=177
177 % 10 = 7
So 1238861-80-7 is a valid CAS Registry Number.

1238861-80-7Downstream Products

1238861-80-7Relevant articles and documents

Microwave-assisted, aqueous wittig reactions: Organic-solvent- And protecting-group-free chemoselective synthesis of functionalized alkenes

McNulty, James,Das, Priyabrata,McLeod, David

, p. 6756 - 6760 (2010)

(Chemical Equation Presented) Free from protection! A general, chemoselective, protecting-group- and organic-solvent-free route to stilbenes and heterostilbenes involving the direct synthesis of triethyl benzylic and allylic phosphonium salts from the corresponding alcohols and their microwave-assisted, aqueous Wittig reactions is described.

Wittig Reactions of Trialkylphosphine-derived Ylides: New Directions and Applications in Organic Synthesis

McNulty, James,McLeod, David,Das, Priyabrata,Zepeda-Velázquez, Carlos

, p. 619 - 632 (2016/01/15)

The development of semi-stabilized, stabilized, and functionalized ylides derived from short-chain trialkylphosphines in the Wittig-type olefination reactions toward the synthesis of alkenes, including stilbenes, styrenes, and 1,3-dienes, as well as reagents for homologation reactions, are described. The methods allow easy access to alkenes with high (E)-stereoselectivity in good yield. These reactions are conducted with weak bases in aqueous media, which allows easy separation of water-soluble phosphine oxides. The development of a mild organocatalytic process for the Wittig reaction and extension toward the preparation of reporter stilbenes under biological conditions are also described. Applications toward the preparation of biologically active natural products and derivatives are discussed.

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