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1-methyl-2-(o-nitrophenyl)indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 58421-66-2 Structure
  • Basic information

    1. Product Name: 1-methyl-2-(o-nitrophenyl)indole
    2. Synonyms: 1-methyl-2-(o-nitrophenyl)indole
    3. CAS NO:58421-66-2
    4. Molecular Formula:
    5. Molecular Weight: 252.272
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 58421-66-2.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: 1-methyl-2-(o-nitrophenyl)indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-methyl-2-(o-nitrophenyl)indole(58421-66-2)
    11. EPA Substance Registry System: 1-methyl-2-(o-nitrophenyl)indole(58421-66-2)
  • 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: 58421-66-2(Hazardous Substances Data)

58421-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58421-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,2 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58421-66:
(7*5)+(6*8)+(5*4)+(4*2)+(3*1)+(2*6)+(1*6)=132
132 % 10 = 2
So 58421-66-2 is a valid CAS Registry Number.

58421-66-2Downstream Products

58421-66-2Relevant articles and documents

Direct C–H Arylation of Heteroarenes with Aryl Chlorides by Using an Abnormal N-Heterocyclic-Carbene–Palladium Catalyst

Ahmed, Jasimuddin,Sau, Samaresh Chandra,Sreejyothi,Hota, Pradip Kumar,Vardhanapu, Pavan K.,Vijaykumar, Gonela,Mandal, Swadhin K.

, p. 1004 - 1011 (2017)

Herein, we report a versatile catalytic system for the direct C–H arylation of heteroarenes with activated aryl chloride substrates. The catalyst works successfully for a variety of heteroarenes and aryl chloride coupling partners under very low catalyst-loading conditions. We have successfully performed the direct C–H arylations of 1-methylpyrrole, 1-methylindole, furan, thiophene, furfural, and N-benzyl-1,2,3-triazole with aryl chloride partners in good yields without the use of any additives. Furthermore, we used this catalytic process to develop a one-pot synthetic protocol for the muscle relaxant dantrolene on a gram scale. Additionally, the present catalytic system can be used to perform consecutive arylations in one pot.

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