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1030513-44-0

4-isobutoxybenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1030513-44-0 Structure

  • Basic information

    1. Product Name: 4-isobutoxybenzamide
    2. Synonyms:
    3. CAS NO:1030513-44-0
    4. Molecular Formula:
    5. Molecular Weight: 193.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1030513-44-0.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: 4-isobutoxybenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-isobutoxybenzamide(1030513-44-0)
    11. EPA Substance Registry System: 4-isobutoxybenzamide(1030513-44-0)

  • 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: 1030513-44-0(Hazardous Substances Data)

1030513-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1030513-44-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,0,5,1 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1030513-44:
(9*1)+(8*0)+(7*3)+(6*0)+(5*5)+(4*1)+(3*3)+(2*4)+(1*4)=80
80 % 10 = 0
So 1030513-44-0 is a valid CAS Registry Number.

1030513-44-0Downstream Products

1030513-44-0Relevant articles and documents

Synthetic method of Pimavanserin

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Paragraph 0006; 0034; 0041-0042; 0051; 0058-0059; 0068, (2019/09/14)

The invention belongs to the field of medicine synthesis, and especially relates to a synthetic method of Pimavanserin. According to the synthetic method, 4-hydroxy benzoic acid is taken as a raw material, esterification reaction, alkylation reaction, hydrolysis, acylation reaction, dehydration reduction, and acylation reaction are carried out to obtain an intermediate (9); fluorobenzylamine and N-methyl-4-piperidone are taken as raw materials for reductive amination to obtain intermediate (10); and at last the intermediate (9) and the intermediate (10) are subjected to aminolysis to obtain finished product Pimavanserin. The initial raw materials are cheap and easily available; reaction conditions are mild; no column chromatography is needed; and the yield is relatively high.

PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF PIMAVANSERIN

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Paragraph 0136, (2018/04/17)

The present disclosure relates to novel, safe and efficient processes for the synthesis of Pimavanserin and salts thereof, as well as novel intermediates that can be used in these processes.

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