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CAS

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1352051-39-8

tert-butyl allyl((4S,5R)-4-allyl-2-phenyl-1,3-dioxan-5-yl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1352051-39-8 Structure

  • Basic information

    1. Product Name: tert-butyl allyl((4S,5R)-4-allyl-2-phenyl-1,3-dioxan-5-yl)carbamate
    2. Synonyms: tert-butyl allyl((4S,5R)-4-allyl-2-phenyl-1,3-dioxan-5-yl)carbamate
    3. CAS NO:1352051-39-8
    4. Molecular Formula:
    5. Molecular Weight: 359.466
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1352051-39-8.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: tert-butyl allyl((4S,5R)-4-allyl-2-phenyl-1,3-dioxan-5-yl)carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl allyl((4S,5R)-4-allyl-2-phenyl-1,3-dioxan-5-yl)carbamate(1352051-39-8)
    11. EPA Substance Registry System: tert-butyl allyl((4S,5R)-4-allyl-2-phenyl-1,3-dioxan-5-yl)carbamate(1352051-39-8)

  • 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: 1352051-39-8(Hazardous Substances Data)

1352051-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1352051-39-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,0,5 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1352051-39:
(9*1)+(8*3)+(7*5)+(6*2)+(5*0)+(4*5)+(3*1)+(2*3)+(1*9)=118
118 % 10 = 8
So 1352051-39-8 is a valid CAS Registry Number.

1352051-39-8Relevant articles and documents

Stereoselective synthesis of (-)-α-conhydrine

Reddipalli, Gowrisankar,Venkataiah, Mallam,Fadnavis, Nitin W.

experimental part, p. 1778 - 1783 (2012/01/04)

(-)-α-Conhydrine was synthesized from propargyl alcohol in 20% overall yield in nine steps. The key intermediates were obtained via a regioselective epoxide opening, cross-metathesis, tandem hydrogenation and hydrogenolysis, and stereoselective dihydroxyl

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