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1,3-bis(morpholin-4-yl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 153529-28-3 Structure
  • Basic information

    1. Product Name: 1,3-bis(morpholin-4-yl)prop-2-en-1-one
    2. Synonyms:
    3. CAS NO:153529-28-3
    4. Molecular Formula:
    5. Molecular Weight: 226.276
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153529-28-3.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: 1,3-bis(morpholin-4-yl)prop-2-en-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-bis(morpholin-4-yl)prop-2-en-1-one(153529-28-3)
    11. EPA Substance Registry System: 1,3-bis(morpholin-4-yl)prop-2-en-1-one(153529-28-3)
  • 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: 153529-28-3(Hazardous Substances Data)

153529-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153529-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,5,2 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 153529-28:
(8*1)+(7*5)+(6*3)+(5*5)+(4*2)+(3*9)+(2*2)+(1*8)=133
133 % 10 = 3
So 153529-28-3 is a valid CAS Registry Number.

153529-28-3Upstream product

153529-28-3Downstream Products

153529-28-3Relevant articles and documents

Efficient tandem synthesis of 3-alkylaminoprop-2-enamides from 3-trimethylsilylprop-2-ynamides

Andreev,Medvedeva,Safronova

, p. 822 - 827 (2013)

A tandem synthetic approach to previously unknown 3-aminoprop-2-enamides has been developed. It is based on Si-C sp desilylation of 3-trimethylsilylprop-2-ynamides and subsequent addition of an amine to the triple bond of intermediate terminal

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