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32121-34-9

methyl 2-(naphthalen-1-yloxy)-2-phenylacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 32121-34-9 Structure

  • Basic information

    1. Product Name: methyl 2-(naphthalen-1-yloxy)-2-phenylacetate
    2. Synonyms: methyl 2-(naphthalen-1-yloxy)-2-phenylacetate
    3. CAS NO:32121-34-9
    4. Molecular Formula:
    5. Molecular Weight: 292.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 32121-34-9.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: methyl 2-(naphthalen-1-yloxy)-2-phenylacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-(naphthalen-1-yloxy)-2-phenylacetate(32121-34-9)
    11. EPA Substance Registry System: methyl 2-(naphthalen-1-yloxy)-2-phenylacetate(32121-34-9)

  • 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: 32121-34-9(Hazardous Substances Data)

32121-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32121-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,2 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32121-34:
(7*3)+(6*2)+(5*1)+(4*2)+(3*1)+(2*3)+(1*4)=59
59 % 10 = 9
So 32121-34-9 is a valid CAS Registry Number.

32121-34-9Downstream Products

32121-34-9Relevant articles and documents

Gold-catalyzed chemoselective formal (3+2)-Annulation reaction between β-naphthols and methyl aryldiazoacetate

Harada, Shingo,Sakai, Chigaya,Tanikawa, Koki,Nemoto, Tetsuhiro

, p. 3650 - 3656 (2019)

A chemoselective domino annulation reaction of β-naphthols with methyl aryldiazoacetate is described. The gold catalyst promoted C–H functionalization of β-naphthols, whereas a rhodium or copper complex led to O–H insertion reactions. Consecutive intramol

Photochemical O-H Functionalization of Aryldiazoacetates with Phenols via Proton Transfer

Empel, Claire,Jana, Sripati,Pei, Chao,Nguyen, Thanh Vinh,Koenigs, Rene M.

supporting information, p. 7225 - 7229 (2020/10/02)

In this work, we report a thorough investigation of the reaction of phenols with aryldiazoacetates. Mechanistic studies using different spectroscopic methods and theoretical calculations suggest a hydrogen bond between phenol and aryldiazoacetates, which can be modulated by the phenol acidity. The pKA of phenol and therefore the hydrogen bond plays an important role in a subsequent photoinduced proton transfer reaction to give the formal O-H functionalization product of phenols.

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