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1427180-43-5

3,5-dimethoxy-N-(pivaloyloxy)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1427180-43-5 Structure

  • Basic information

    1. Product Name: 3,5-dimethoxy-N-(pivaloyloxy)benzamide
    2. Synonyms: 3,5-dimethoxy-N-(pivaloyloxy)benzamide
    3. CAS NO:1427180-43-5
    4. Molecular Formula:
    5. Molecular Weight: 281.309
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1427180-43-5.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: 3,5-dimethoxy-N-(pivaloyloxy)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-dimethoxy-N-(pivaloyloxy)benzamide(1427180-43-5)
    11. EPA Substance Registry System: 3,5-dimethoxy-N-(pivaloyloxy)benzamide(1427180-43-5)

  • 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: 1427180-43-5(Hazardous Substances Data)

1427180-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427180-43-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,1,8 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1427180-43:
(9*1)+(8*4)+(7*2)+(6*7)+(5*1)+(4*8)+(3*0)+(2*4)+(1*3)=145
145 % 10 = 5
So 1427180-43-5 is a valid CAS Registry Number.

1427180-43-5Downstream Products

1427180-43-5Relevant articles and documents

Formal Lossen Rearrangement/[3+2] Annulation Cascade Catalyzed by a Modified Cyclopentadienyl RhIII Complex

Yamada, Takayuki,Shibata, Yu,Kawauchi, Susumu,Yoshizaki, Soichi,Tanaka, Ken

supporting information, p. 5723 - 5727 (2018/04/11)

It has been established that a cyclopentadienyl RhIII complex with two phenyl groups and a pendant amide moiety catalyzes the formal Lossen rearrangement/[3+2] annulation cascade of N-pivaloyl benzamides and acrylamides with alkynes leading to substituted indoles and pyrroles. Mechanistic studies revealed that this cascade reaction proceeds via not the Lossen rearrangement to form anilides or enamides but C?H bond cleavage, alkyne insertion, and the formal Lossen rearrangement.

Complementary regioselectivity in Rh(III)-catalyzed insertions of potassium vinyltrifluoroborate via C-H activation: Preparation and use of 4-trifluoroboratotetrahydroisoquinolones

Presset, Marc,Oehlrich, Daniel,Rombouts, Frederik,Molander, Gary A.

, p. 1528 - 1531 (2013/06/27)

Potassium vinyltrifluoroborate was found to be an efficient partner with benzamide derivatives for Rh(III)-catalyzed annulations. 4- Trifluoroboratotetrahydroisoquinolones were generated under mild conditions, affording a regioisomerically complementary substitution pattern to other alkenes in related reactions. These new boron-containing building blocks were derivatized by N-arylations, retaining the boron substituent for further elaboration.

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