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73111-07-6

Phenol, 4-(3,4-dihydro-2H-1-benzopyran-2-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 73111-07-6 Structure

  • Basic information

    1. Product Name: Phenol, 4-(3,4-dihydro-2H-1-benzopyran-2-yl)-
    2. Synonyms:
    3. CAS NO:73111-07-6
    4. Molecular Formula: C15H14O2
    5. Molecular Weight: 226.275
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73111-07-6.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: Phenol, 4-(3,4-dihydro-2H-1-benzopyran-2-yl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenol, 4-(3,4-dihydro-2H-1-benzopyran-2-yl)-(73111-07-6)
    11. EPA Substance Registry System: Phenol, 4-(3,4-dihydro-2H-1-benzopyran-2-yl)-(73111-07-6)

  • 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: 73111-07-6(Hazardous Substances Data)

73111-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73111-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,1 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73111-07:
(7*7)+(6*3)+(5*1)+(4*1)+(3*1)+(2*0)+(1*7)=86
86 % 10 = 6
So 73111-07-6 is a valid CAS Registry Number.

73111-07-6Downstream Products

73111-07-6Relevant articles and documents

One-Pot Synthesis of O-Heterocycles or Aryl Ketones Using an InCl3/Et3SiH System by Switching the Solvent

Jia, Wenqiang,Xi, Qiumu,Liu, Tianqi,Yang, Minjian,Chen, Yonghui,Yin, Dali,Wang, Xiaojian

, p. 5141 - 5149 (2019)

An efficient one-pot synthesis of O-heterocycles or aryl ketones has been achieved using Et3SiH in the presence of InCl3 via a sequential ionic hydrogenation reaction by switching the solvent. This methodology can be used to construct C-O bonds and to prepare conjugate reduction products, including chromans, tetrahydrofurans, tetrahydropyrans, dihydroisobenzofurans, dihydrochalcones, and 1,4-diones in a facile manner. In addition, a novel plausible mechanism involving a conjugate reduction and a tandem reductive cyclization was verified by experimental investigations.

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