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152386-86-2

(2R,3R,4E)-1,2-O-pentylidene-3-(4-methoxybenzyl)-4-octadecen-1,2,3-triol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 152386-86-2 Structure

  • Basic information

    1. Product Name: (2R,3R,4E)-1,2-O-pentylidene-3-(4-methoxybenzyl)-4-octadecen-1,2,3-triol
    2. Synonyms: (2R,3R,4E)-1,2-O-pentylidene-3-(4-methoxybenzyl)-4-octadecen-1,2,3-triol
    3. CAS NO:152386-86-2
    4. Molecular Formula:
    5. Molecular Weight: 488.751
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 152386-86-2.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,3R,4E)-1,2-O-pentylidene-3-(4-methoxybenzyl)-4-octadecen-1,2,3-triol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R,4E)-1,2-O-pentylidene-3-(4-methoxybenzyl)-4-octadecen-1,2,3-triol(152386-86-2)
    11. EPA Substance Registry System: (2R,3R,4E)-1,2-O-pentylidene-3-(4-methoxybenzyl)-4-octadecen-1,2,3-triol(152386-86-2)

  • 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: 152386-86-2(Hazardous Substances Data)

152386-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152386-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,3,8 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 152386-86:
(8*1)+(7*5)+(6*2)+(5*3)+(4*8)+(3*6)+(2*8)+(1*6)=142
142 % 10 = 2
So 152386-86-2 is a valid CAS Registry Number.

152386-86-2Relevant articles and documents

A formal synthesis of 3-O-(4-methoxybenzyl)-azidosphingosine by a modified Julia olefination

Compostella, Federica,Franchini, Laura,Panza, Luigi,Prosperi, Davide,Ronchetti, Fiamma

, p. 4425 - 4428 (2007/10/03)

The stereoselective construction of the D-erythro-azidosphingosine characteristic trans double bond was accomplished by condensation between tetradecanal and a heterocyclic sulfone derived from diethyl-D-tartrate, following the Kocienski modification of the Julia olefination.

An enantiospecific synthesis of D-erythro-sphingosine from D-tartaric acid

Somfai, Peter,Olsson, Roger

, p. 6645 - 6650 (2007/10/02)

An efficient enantiospecific synthesis of D-erythro-sphingosine (1) via azidosphingosine (2) is described, the absolute stereochemistry being derived from D-tartaric acid.

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