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CAS

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1280572-71-5

(1R,2R,3S)-2-(hydroxymethyl)-3-isopropyl-1-methylcyclopentanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1280572-71-5 Structure

  • Basic information

    1. Product Name: (1R,2R,3S)-2-(hydroxymethyl)-3-isopropyl-1-methylcyclopentanol
    2. Synonyms:
    3. CAS NO:1280572-71-5
    4. Molecular Formula:
    5. Molecular Weight: 172.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1280572-71-5.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: (1R,2R,3S)-2-(hydroxymethyl)-3-isopropyl-1-methylcyclopentanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,2R,3S)-2-(hydroxymethyl)-3-isopropyl-1-methylcyclopentanol(1280572-71-5)
    11. EPA Substance Registry System: (1R,2R,3S)-2-(hydroxymethyl)-3-isopropyl-1-methylcyclopentanol(1280572-71-5)

  • 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: 1280572-71-5(Hazardous Substances Data)

1280572-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1280572-71-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,0,5,7 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1280572-71:
(9*1)+(8*2)+(7*8)+(6*0)+(5*5)+(4*7)+(3*2)+(2*7)+(1*1)=155
155 % 10 = 5
So 1280572-71-5 is a valid CAS Registry Number.

1280572-71-5Downstream Products

1280572-71-5Relevant articles and documents

Protecting-group-free synthesis of chokols

Morales, Carmen Perez,Catalan, Julieta,Domingo, Victoriano,Gonzalez Delgado, Jose A.,Dobado, Jose A.,Herrador, M. Mar,Quilez Del Moral, Jose F.,Barrero, Alejandro F.

supporting information; experimental part, p. 2494 - 2501 (2011/06/20)

As a result of a combined theoretical and experimental study, we describe a two-step protocol for the preparation of an optically pure, multifunctional, cyclopentanic core shared by a number of natural products. This process is based on a hitherto unreported Ti(III)-mediated diastereoselective cyclization in which the hydroxy-directed template effect played by the Ti(III) species was found to be crucial for the stereoselective outcome of the reaction. The viability of this concept was confirmed with the first protecting-group free synthesis of three enantiopure chokols, namely, chokols K, E, and B.

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