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134252-16-7

1-hydroxy-2-propanone oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134252-16-7 Structure

  • Basic information

    1. Product Name: 1-hydroxy-2-propanone oxime
    2. Synonyms: 1-hydroxy-2-propanone oxime
    3. CAS NO:134252-16-7
    4. Molecular Formula:
    5. Molecular Weight: 89.0941
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134252-16-7.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: 1-hydroxy-2-propanone oxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-hydroxy-2-propanone oxime(134252-16-7)
    11. EPA Substance Registry System: 1-hydroxy-2-propanone oxime(134252-16-7)

  • 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: 134252-16-7(Hazardous Substances Data)

134252-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134252-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,2,5 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 134252-16:
(8*1)+(7*3)+(6*4)+(5*2)+(4*5)+(3*2)+(2*1)+(1*6)=97
97 % 10 = 7
So 134252-16-7 is a valid CAS Registry Number.

134252-16-7Relevant articles and documents

Kinetics and Mechanism of the Alkaline Release of Phenyl(mercapto)tetrazoles from α-Oximes

Boggs, Roger A.,Hasan, Fariza B.,Mahoney, J. Barry,Mehta, Avi C.,Palumbo, Catherine M. K.,et al.

, p. 1271 - 1277 (2007/10/02)

Compounds such as α-phenyl(mercapto)tetrazole (PMT) oxime (9) undergo rapid elimination of the PMT anion in base via a nitrosoene intermediate.Solution kinetics and HPLC analysis of reaction products are consistent with the mechanism shown in Scheme 2.For open chain oximes such as 4, substitution α to the oxime increases the rate of release of PMT and is attributed to the relief of strain when a crowded reactant is converted to a less-crowded product.For cyclic oximes, the six-membered ring compounds are more reactive than the corresponding five-membered compounds.A linear isokinetic relationship between the entropy and enthalpy of activation was found with β = 346 +/- 51 K.Entropies of activation were found to range from -7 to +24 c.u. (1 c.u. = 4.184 J mol-1 K-1) and support the proposed mechanism.

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