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3-isopropyl-5-(4-methoxyphenyl)isoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1346238-46-7 Structure
  • Basic information

    1. Product Name: 3-isopropyl-5-(4-methoxyphenyl)isoxazole
    2. Synonyms: 3-isopropyl-5-(4-methoxyphenyl)isoxazole
    3. CAS NO:1346238-46-7
    4. Molecular Formula:
    5. Molecular Weight: 217.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1346238-46-7.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: 3-isopropyl-5-(4-methoxyphenyl)isoxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-isopropyl-5-(4-methoxyphenyl)isoxazole(1346238-46-7)
    11. EPA Substance Registry System: 3-isopropyl-5-(4-methoxyphenyl)isoxazole(1346238-46-7)
  • 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: 1346238-46-7(Hazardous Substances Data)

1346238-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1346238-46-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,2,3 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1346238-46:
(9*1)+(8*3)+(7*4)+(6*6)+(5*2)+(4*3)+(3*8)+(2*4)+(1*6)=157
157 % 10 = 7
So 1346238-46-7 is a valid CAS Registry Number.

1346238-46-7Downstream Products

1346238-46-7Relevant articles and documents

In Situ Generation of Nitrile Oxides from NaCl-Oxone Oxidation of Various Aldoximes and Their 1,3-Dipolar Cycloaddition

Zhao, Guodong,Liang, Lixin,Wen, Chi Ho Ethan,Tong, Rongbiao

, p. 315 - 319 (2019)

Reported is a new green protocol for the efficient in situ generation of nitrile oxides through NaCl/Oxone oxidation of aldoximes and their dipolar cycloaddition. The key feature is the use of a green chemistry approach to address the substrate scope of aldoximes: broad scope (aliphatic, aromatic, and alkenyl aldoximes) without production of organic byproducts derived from oxidant and/or catalyst. Importantly, NaCl/Oxone-promoted three-component cycloaddition of aldehyde, hydroxylamine hydrochloride, and alkene was demonstrated to be competent (63-81%).

Transition metal-free TEMPO-catalyzed oxidative cross-coupling of nitrones with alkynyl-grignard reagents

Murarka, Sandip,Studer, Armido

, p. 2708 - 2714 (2011/12/05)

An efficient mild one-pot protocol for the cross-coupling of nitrones and alkynyl-magnesium compounds using a catalytic amount of 2,2,6,6- tetramethylpiperidine-N-oxyl radical (TEMPO) as an environmentally benign organic oxidant and dioxygen as terminal o

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