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1021154-59-5

methyl 1-cyclopropyl-1H-indole-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1021154-59-5 Structure

  • Basic information

    1. Product Name: methyl 1-cyclopropyl-1H-indole-3-carboxylate
    2. Synonyms: methyl 1-cyclopropyl-1H-indole-3-carboxylate
    3. CAS NO:1021154-59-5
    4. Molecular Formula: C13H13NO2
    5. Molecular Weight: 215.24782
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1021154-59-5.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: methyl 1-cyclopropyl-1H-indole-3-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 1-cyclopropyl-1H-indole-3-carboxylate(1021154-59-5)
    11. EPA Substance Registry System: methyl 1-cyclopropyl-1H-indole-3-carboxylate(1021154-59-5)

  • 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: 1021154-59-5(Hazardous Substances Data)

1021154-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1021154-59-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,1,1,5 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1021154-59:
(9*1)+(8*0)+(7*2)+(6*1)+(5*1)+(4*5)+(3*4)+(2*5)+(1*9)=85
85 % 10 = 5
So 1021154-59-5 is a valid CAS Registry Number.

1021154-59-5Downstream Products

1021154-59-5Relevant articles and documents

Synthesis of indoles via electron-catalyzed intramolecular C?N bond formation

Bugaenko, Dmitry I.,Dubrovina, Anastasia A.,Yurovskaya, Marina A.,Karchava, Alexander V.

supporting information, p. 7358 - 7362 (2018/12/13)

A new protocol for the preparation of N-substituted indole-3-carboxylates has been developed. The key C?N bond formation occurs under transition-metal-free conditions employing a t-BuOK/DMF system without special initiators or additives. Across a number o

N-cyclopropylation of indoles and cyclic amides with copper(II) reagent

Tsuritani, Takayuki,Strotman, Neil A.,Yamamoto, Yuhei,Kawasaki, Masashi,Yasuda, Nobuyoshi,Mase, Toshiaki

supporting information; experimental part, p. 1653 - 1655 (2009/04/07)

Copper-mediated coupling reactions of cyclopropylboronic acid with indoles and cyclic amides are described. The process utilizes catalytic or stoichiometric amounts of copper(ll) acetate, DMAP, and NaHMDS at 95 °C under an atmosphere containing oxygen. A variety of functional groups remain intact throughout the reaction.

Synthesis of N-substituted indole-3-carboxylic acid derivatives via Cu(I)-catalyzed intramolecular amination of aryl bromides

Melkonyan, Ferdinand S.,Karchava, Alexander V.,Yurovskaya, Marina A.

, p. 4275 - 4278 (2008/09/20)

(Chemical Equation Presented) A variety of N-alkylated and N-arylated derivatives of methyl 1H-indole-3-carboxylate were synthesized efficiently via Ullmann-type intramolecular arylamination, using the CuI-K3PO 4-DMF system. This cat

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