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ethyl 4-(4-methoxybenzamido)-2-oxo-4-phenylbutanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1312310-26-1 Structure
  • Basic information

    1. Product Name: ethyl 4-(4-methoxybenzamido)-2-oxo-4-phenylbutanoate
    2. Synonyms: ethyl 4-(4-methoxybenzamido)-2-oxo-4-phenylbutanoate
    3. CAS NO:1312310-26-1
    4. Molecular Formula:
    5. Molecular Weight: 355.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1312310-26-1.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: ethyl 4-(4-methoxybenzamido)-2-oxo-4-phenylbutanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 4-(4-methoxybenzamido)-2-oxo-4-phenylbutanoate(1312310-26-1)
    11. EPA Substance Registry System: ethyl 4-(4-methoxybenzamido)-2-oxo-4-phenylbutanoate(1312310-26-1)
  • 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: 1312310-26-1(Hazardous Substances Data)

1312310-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1312310-26-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,3,1 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1312310-26:
(9*1)+(8*3)+(7*1)+(6*2)+(5*3)+(4*1)+(3*0)+(2*2)+(1*6)=81
81 % 10 = 1
So 1312310-26-1 is a valid CAS Registry Number.

1312310-26-1Downstream Products

1312310-26-1Relevant articles and documents

Catalytic syntheses of γ-functionalized α-keto esters from thioacetals and N,O-acetals

Krebs, Anke,Bolm, Carsten

, p. 4055 - 4060 (2011)

Ethyl 2-(trimethylsilyloxy)acrylic ester (1a) reacts with thioacetals providing the corresponding α-keto-γ-thio esters in good to satisfactory yields. Whereas aminals do not react, N,O-acetals lead to γ-amino-α-keto esters in good to excellent yields. All reactions proceed under mild reaction conditions, and no additional work up is required. Subsequent transformations of the obtained products to the corresponding α-oximes have been demonstrated.

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