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121470-05-1

(S)-((pent-4-en-2-yloxy)methyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 121470-05-1 Structure

  • Basic information

    1. Product Name: (S)-((pent-4-en-2-yloxy)methyl)benzene
    2. Synonyms:
    3. CAS NO:121470-05-1
    4. Molecular Formula:
    5. Molecular Weight: 176.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121470-05-1.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: (S)-((pent-4-en-2-yloxy)methyl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-((pent-4-en-2-yloxy)methyl)benzene(121470-05-1)
    11. EPA Substance Registry System: (S)-((pent-4-en-2-yloxy)methyl)benzene(121470-05-1)

  • 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: 121470-05-1(Hazardous Substances Data)

121470-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121470-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,4,7 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 121470-05:
(8*1)+(7*2)+(6*1)+(5*4)+(4*7)+(3*0)+(2*0)+(1*5)=81
81 % 10 = 1
So 121470-05-1 is a valid CAS Registry Number.

121470-05-1Relevant articles and documents

Total Synthesis of Tetraketide and Cryptorigidifoliol i via a Sequential Allylation Strategy

Padhi, Birakishore,Reddy, G. Sudhakar,Mohapatra, Debendra K.

, p. 2788 - 2796 (2016)

A unified and efficient synthetic route for both tetraketide (1) and cryptorigidifoliol I (2) has been devised successfully from commercially available starting materials in 11 and 17 steps, with 16% and 11% overall yields, respectively. Highlights of the syntheses involved sequential Lewis acid-catalyzed highly regio- and diastereoselective allylations and intramolecular Mitsunobu lactonization.

Total syntheses of the resorcylic acid lactones paecilomycin F and cochliomycin C using an intramolecular loh-type α-allylation reaction for macrolide formation

Ma, Xiang,Bolte, Benoit,Banwell, Martin G.,Willis, Anthony C.

, p. 4226 - 4229 (2016)

Subjection of the resorcylic ester 16 to a Nozaki-Hiyama-Kishi reaction afforded the 12-membered lactone 17, while treatment of it under the Loh-type α-allylation conditions using indium metal gave the isomeric, 14-membered macrolide 18. Compound 18 was readily elaborated to the resorcylic acid lactone type natural products paecilomycin F and cochliomycin C.

Chiral Building Units from Carbohydrates, VIII. - Syntheses of the Four Isomeric 1,3-Dimethyl-2,9-dioxabicyclononanes

Redlich, Hartmut,Schneider, Bernd,Hoffmann, Reinhard W.,Geueke, Karl-Josef

, p. 393 - 411 (2007/10/02)

Starting from different compounds, the syntheses of the four isomeric bicyclic acetals 17, 32, 36, and 40 - the title compounds - are described.One of these compounds is supposed to direct the attack of the striped ambrosia beetle Trypodendron lineatum Ol

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