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1-methoxy-5-methyl-hexan-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 53704-54-4 Structure
  • Basic information

    1. Product Name: 1-methoxy-5-methyl-hexan-3-one
    2. Synonyms: 1-methoxy-5-methyl-hexan-3-one
    3. CAS NO:53704-54-4
    4. Molecular Formula:
    5. Molecular Weight: 144.214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53704-54-4.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-methoxy-5-methyl-hexan-3-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-methoxy-5-methyl-hexan-3-one(53704-54-4)
    11. EPA Substance Registry System: 1-methoxy-5-methyl-hexan-3-one(53704-54-4)
  • 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: 53704-54-4(Hazardous Substances Data)

53704-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53704-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,0 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53704-54:
(7*5)+(6*3)+(5*7)+(4*0)+(3*4)+(2*5)+(1*4)=114
114 % 10 = 4
So 53704-54-4 is a valid CAS Registry Number.

53704-54-4Relevant articles and documents

Iron-catalyzed urea synthesis: Dehydrogenative coupling of methanol and amines

Lane, Elizabeth M.,Hazari, Nilay,Bernskoetter, Wesley H.

, p. 4003 - 4008 (2018)

Substituted ureas have numerous applications but their synthesis typically requires the use of highly toxic starting materials. Herein we describe the first base-metal catalyst for the selective synthesis of symmetric ureas via the dehydrogenative coupling of methanol with primary amines. Using a pincer supported iron catalyst, a range of ureas was generated with isolated yields of up to 80% (corresponding to a catalytic turnover of up to 160) and with H2 as the sole byproduct. Mechanistic studies indicate a stepwise pathway beginning with methanol dehydrogenation to give formaldehyde, which is trapped by amine to afford a formamide. The formamide is then dehydrogenated to produce a transient isocyanate, which reacts with another equivalent of amine to form a urea. These mechanistic insights enabled the development of an iron-catalyzed method for the synthesis of unsymmetric ureas from amides and amines.

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