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1-(2-ethyl-4,5-dimethoxyphenyl)-1-propanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92156-94-0 Structure
  • Basic information

    1. Product Name: 1-(2-ethyl-4,5-dimethoxyphenyl)-1-propanone
    2. Synonyms: 1-(2-ethyl-4,5-dimethoxyphenyl)-1-propanone
    3. CAS NO:92156-94-0
    4. Molecular Formula:
    5. Molecular Weight: 222.284
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92156-94-0.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: 1-(2-ethyl-4,5-dimethoxyphenyl)-1-propanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-ethyl-4,5-dimethoxyphenyl)-1-propanone(92156-94-0)
    11. EPA Substance Registry System: 1-(2-ethyl-4,5-dimethoxyphenyl)-1-propanone(92156-94-0)
  • 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: 92156-94-0(Hazardous Substances Data)

92156-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92156-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,5 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92156-94:
(7*9)+(6*2)+(5*1)+(4*5)+(3*6)+(2*9)+(1*4)=140
140 % 10 = 0
So 92156-94-0 is a valid CAS Registry Number.

92156-94-0Relevant articles and documents

Synthesis and anti-inflammatory activity of 1-acylaminoalkyl-3,4- dialkoxybenzene derivatives

Labanauskas,Brukstus,Udrenaite,Bucinskaite,Susvilo,Urbelis

, p. 203 - 207 (2007/10/03)

New 1-acylaminoalkyl-3,4-dialkoxybenzene derivatives 17-31 were synthesized by the acylation of amines 9-16 with acyl chlorides. Amines 9-16 were obtained from aryl ketones 1-8. Aryl ketones 1-8 were synthesized by the acylation of corresponding aromatic

An efficient method for the synthesis of 4,5-disubstituted catechols

Ma, Tingli,Kojima, Takahiko,Matsuda, Yoshihisa

, p. 747 - 748 (2007/10/03)

4,5-Disubstituted catechols were prepared in high yields via successive Friedel-Crafts acylation in the presence of a Ti(IV) catalyst or I2 and reduction with triethylsilane of veratroles. This method provides an effective and well-regulated synthetic strategy toward catechol derivatives having a variety of substituents at the 4- and 5- positions.

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