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CAS

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1058213-80-1

triethyl (Z,2S,3R)-(3-isopropyl-5-phenylpent-4-en-2-yloxy)silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1058213-80-1 Structure

  • Basic information

    1. Product Name: triethyl (Z,2S,3R)-(3-isopropyl-5-phenylpent-4-en-2-yloxy)silane
    2. Synonyms: triethyl (Z,2S,3R)-(3-isopropyl-5-phenylpent-4-en-2-yloxy)silane
    3. CAS NO:1058213-80-1
    4. Molecular Formula:
    5. Molecular Weight: 318.575
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1058213-80-1.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: triethyl (Z,2S,3R)-(3-isopropyl-5-phenylpent-4-en-2-yloxy)silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: triethyl (Z,2S,3R)-(3-isopropyl-5-phenylpent-4-en-2-yloxy)silane(1058213-80-1)
    11. EPA Substance Registry System: triethyl (Z,2S,3R)-(3-isopropyl-5-phenylpent-4-en-2-yloxy)silane(1058213-80-1)

  • 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: 1058213-80-1(Hazardous Substances Data)

1058213-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1058213-80-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,8,2,1 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1058213-80:
(9*1)+(8*0)+(7*5)+(6*8)+(5*2)+(4*1)+(3*3)+(2*8)+(1*0)=131
131 % 10 = 1
So 1058213-80-1 is a valid CAS Registry Number.

1058213-80-1Downstream Products

1058213-80-1Relevant articles and documents

Anionic cross-coupling reaction of α-metallated alkenyl sulfoximines and alkenyl sulfoximines with cuprates featuring a 1,2-metal-ate rearrangement of sulfoximine-substituted higher order alkenyl cuprates and an α-metallation of alkenyl sulfoximines by cuprates

Gais, Hans-Joachim,Rao, C. Venkateshwar,Loo, Ralf

experimental part, p. 6510 - 6528 (2009/06/18)

(E)- and (Z)-configured αlithioalkenyl sulfoximines, which are available through lithiation of the corresponding alkenyl sulfoximines, undergo a anionic cross-coupling reaction (ACCR) with organocuprates with formation of the corresponding alkenyl cuprates and sulfinamide. The alkenyl cuprates can be trapped by electrophiles. The ACCR presumably proceeds via the formation of a higher-order sulfoximine-substituted alkenyl cuprate, which undergoes a 1,2-metalate rearrangement whereby the sulfoximine group acts as the nucleofuge. The parent (E)- and (Z)-configured alkenyl sulfoximines suffer upon treatment with an organocuprate a deprotonation at the α-position with formation of the corresponding α-cuprioalkenyl sulfoximines. These derivatives also enter into a similar ACCR with organocuprates. The ACCR of sulfoximines substituted homoallylic alcohols allows a stereoselective access to enantio- and diastereopure substituted homoallylic alcohols.

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