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160422-65-1

Phenyl-carbamic acid 2-hydroperoxy-3-phenyl-but-3-enyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 160422-65-1 Structure

  • Basic information

    1. Product Name: Phenyl-carbamic acid 2-hydroperoxy-3-phenyl-but-3-enyl ester
    2. Synonyms:
    3. CAS NO:160422-65-1
    4. Molecular Formula:
    5. Molecular Weight: 299.326
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160422-65-1.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: Phenyl-carbamic acid 2-hydroperoxy-3-phenyl-but-3-enyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenyl-carbamic acid 2-hydroperoxy-3-phenyl-but-3-enyl ester(160422-65-1)
    11. EPA Substance Registry System: Phenyl-carbamic acid 2-hydroperoxy-3-phenyl-but-3-enyl ester(160422-65-1)

  • 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: 160422-65-1(Hazardous Substances Data)

160422-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160422-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,4,2 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 160422-65:
(8*1)+(7*6)+(6*0)+(5*4)+(4*2)+(3*2)+(2*6)+(1*5)=101
101 % 10 = 1
So 160422-65-1 is a valid CAS Registry Number.

160422-65-1Downstream Products

160422-65-1Relevant articles and documents

6-hydroxymethyl-1,2,4-trioxanes and derivatives: An alternative 1,2,4-trioxane synthesis from β′γ′-unsaturated β-hydroxyhydroperoxides

Bloodworth,Johnson, Karen A.

, p. 8057 - 8060 (2007/10/02)

Allylic hydroperoxides CH2:C(Ph)CH(OOH)CH2OX (X = H, CONHPh, Ac), from regiospecific photooxygenation of allylic alcohols CH3C(Ph):CHCH2OX, form hemiperoxyacetals with aldehydes or ketones which upon cyclisation with mercury(II) trifluoroacetate then reduction with sodium borohydride diastereoselectively afford 1,2,4-trioxanes with XOCH2 substituents at C-6.

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