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  • 1224199-09-0 Structure
  • Basic information

    1. Product Name: C13H14O3
    2. Synonyms: C13H14O3
    3. CAS NO:1224199-09-0
    4. Molecular Formula:
    5. Molecular Weight: 218.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1224199-09-0.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: C13H14O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H14O3(1224199-09-0)
    11. EPA Substance Registry System: C13H14O3(1224199-09-0)
  • 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: 1224199-09-0(Hazardous Substances Data)

1224199-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1224199-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,1,9 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1224199-09:
(9*1)+(8*2)+(7*2)+(6*4)+(5*1)+(4*9)+(3*9)+(2*0)+(1*9)=140
140 % 10 = 0
So 1224199-09-0 is a valid CAS Registry Number.

1224199-09-0Downstream Products

1224199-09-0Relevant articles and documents

CHEMICALLY STABLE LIGNIN DERIVATIVE AND METHOD FOR PREPARING SAME

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Paragraph 0148-0150; 0165-0179, (2020/12/19)

A lignin derivative including a unit of general formula (I): in which R1, R2, R3 and R4, which may be identical or different, each represent a hydrogen atom, a methoxy group —OMe, a hydroxyl group, where appropriate protected by a protective group of a hydroxyl function, or a unit R5 represents a hydrogen atom, a protective group of a hydroxyl function or a unit; A represents an oxygen atom, a sulfur atom, an —NH group or an —NR′ group; and R′1, R′2, R′3 and R′4 each represent a hydrogen atom or a substituent not including a mesomeric-effect electron-withdrawing group conjugated to the aromatic ring, a substituent from R′1, R′2, R′3 and R′4 representing the covalent bond with the benzylic carbon.

Organocatalyzed Friedel-Crafts arylation of benzylic alcohols

McCubbin, J. Adam,Krokhin, Oleg V.

supporting information; experimental part, p. 2447 - 2449 (2010/07/04)

Electron-rich aromatic and heteroaromatic rings are functionalized directly with a variety of benzylic alcohols under mild conditions. The reaction is catalyzed by commercially available pentafluorophenylboronic acid, which is stable under ambient conditions and recoverable. The reaction itself is highly atom economical and produces water as the only byproduct. A Friedel-Crafts mechanism is proposed.

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