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291530-55-7

2-(S)-hydroxypropyl propenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 291530-55-7 Structure

  • Basic information

    1. Product Name: 2-(S)-hydroxypropyl propenoate
    2. Synonyms:
    3. CAS NO:291530-55-7
    4. Molecular Formula:
    5. Molecular Weight: 130.144
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 291530-55-7.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: 2-(S)-hydroxypropyl propenoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(S)-hydroxypropyl propenoate(291530-55-7)
    11. EPA Substance Registry System: 2-(S)-hydroxypropyl propenoate(291530-55-7)

  • 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: 291530-55-7(Hazardous Substances Data)

291530-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 291530-55-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,1,5,3 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 291530-55:
(8*2)+(7*9)+(6*1)+(5*5)+(4*3)+(3*0)+(2*5)+(1*5)=137
137 % 10 = 7
So 291530-55-7 is a valid CAS Registry Number.

291530-55-7Relevant articles and documents

Diastereoselective synthesis of bis(3,5)pyrazolophanes by sequential inter- and intramolecular cycloadditions of homochiral nitrilimines

Broggini, Gianluigi,Molteni, Giorgio,Pilati, Tullio

, p. 1975 - 1983 (2000)

Starting from ethyl (S)-lactate as the chiral unit, we have developed the synthesis of the enantiopure bis(3,5)pyrazolophanes 9 and 19 by means of sequential inter- and intramolecular cycloadditions of nitrilimine intermediates. Copyright (C) 2000 Elsevie

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