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CAS

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144866-83-1

(2R,3E)-(-)-1-methylamino-2-(2'-phenoxy-isopropyl)oxypentene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144866-83-1 Structure

  • Basic information

    1. Product Name: (2R,3E)-(-)-1-methylamino-2-(2'-phenoxy-isopropyl)oxypentene
    2. Synonyms:
    3. CAS NO:144866-83-1
    4. Molecular Formula:
    5. Molecular Weight: 249.353
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144866-83-1.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: (2R,3E)-(-)-1-methylamino-2-(2'-phenoxy-isopropyl)oxypentene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3E)-(-)-1-methylamino-2-(2'-phenoxy-isopropyl)oxypentene(144866-83-1)
    11. EPA Substance Registry System: (2R,3E)-(-)-1-methylamino-2-(2'-phenoxy-isopropyl)oxypentene(144866-83-1)

  • 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: 144866-83-1(Hazardous Substances Data)

144866-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144866-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,8,6 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 144866-83:
(8*1)+(7*4)+(6*4)+(5*8)+(4*6)+(3*6)+(2*8)+(1*3)=161
161 % 10 = 1
So 144866-83-1 is a valid CAS Registry Number.

144866-83-1Downstream Products

144866-83-1Relevant articles and documents

2-Phenoxypropene as protective reagent of chiral alcohols

Zandbergen,Willems,Van der Marel,Brussee,Van der Gen

, p. 2781 - 2787 (2007/10/02)

2-Phenoxypropene (2) was applied as a novel protective reagent of chiral alcohols, yielding 2-phenoxy-isopropyl (PIP) ethers. Introduction and cleavage of the protective group was achieved under mild conditions.

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