Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1058213-82-3

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

1058213-82-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1058213-82-3 Structure

  • Basic information

    1. Product Name: (E,2S,3R)-3-isopropyl-5-phenylpent-4-en-2-ol
    2. Synonyms: (E,2S,3R)-3-isopropyl-5-phenylpent-4-en-2-ol
    3. CAS NO:1058213-82-3
    4. Molecular Formula:
    5. Molecular Weight: 204.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1058213-82-3.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: (E,2S,3R)-3-isopropyl-5-phenylpent-4-en-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E,2S,3R)-3-isopropyl-5-phenylpent-4-en-2-ol(1058213-82-3)
    11. EPA Substance Registry System: (E,2S,3R)-3-isopropyl-5-phenylpent-4-en-2-ol(1058213-82-3)

  • 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: 1058213-82-3(Hazardous Substances Data)

1058213-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1058213-82-3 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 1058213-82:
(9*1)+(8*0)+(7*5)+(6*8)+(5*2)+(4*1)+(3*3)+(2*8)+(1*2)=133
133 % 10 = 3
So 1058213-82-3 is a valid CAS Registry Number.

1058213-82-3Downstream Products

1058213-82-3Relevant 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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1058213-82-3