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CAS

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20134-99-0

propanal oxime propyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 20134-99-0 Structure

  • Basic information

    1. Product Name: propanal oxime propyl ether
    2. Synonyms:
    3. CAS NO:20134-99-0
    4. Molecular Formula:
    5. Molecular Weight: 115.175
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20134-99-0.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: propanal oxime propyl ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: propanal oxime propyl ether(20134-99-0)
    11. EPA Substance Registry System: propanal oxime propyl ether(20134-99-0)

  • 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: 20134-99-0(Hazardous Substances Data)

20134-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20134-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,3 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20134-99:
(7*2)+(6*0)+(5*1)+(4*3)+(3*4)+(2*9)+(1*9)=70
70 % 10 = 0
So 20134-99-0 is a valid CAS Registry Number.

20134-99-0Downstream Products

20134-99-0Relevant articles and documents

FORMATION OF NITROSO COMPOUNDS AND OXIME ETHERS DURING OXIDATION OF ALKOXYAMINES

Ioffe, B. V.,Artsybasheva, Yu. P.

, p. 795 - 798 (2007/10/02)

The O-alkyl ethers of oximes, which are always present among the products from oxidation of alkoxyamines under mild conditions, must be regarded as the result from rearrangement of the intermediate alkoxynitrenes to nitroso compounds and oximes with conversion of the latter into the corresponding ethers by the action of an excess of the alkoxyamine.

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