Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1154743-94-8

(+)-(3S,4E)-3-phenylhex-4-enoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1154743-94-8 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1154743-94-8 Structure

  • Basic information

    1. Product Name: (+)-(3S,4E)-3-phenylhex-4-enoic acid
    2. Synonyms: (+)-(3S,4E)-3-phenylhex-4-enoic acid
    3. CAS NO:1154743-94-8
    4. Molecular Formula:
    5. Molecular Weight: 190.242
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1154743-94-8.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: (+)-(3S,4E)-3-phenylhex-4-enoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+)-(3S,4E)-3-phenylhex-4-enoic acid(1154743-94-8)
    11. EPA Substance Registry System: (+)-(3S,4E)-3-phenylhex-4-enoic acid(1154743-94-8)

  • 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: 1154743-94-8(Hazardous Substances Data)

1154743-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1154743-94-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,4,7,4 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1154743-94:
(9*1)+(8*1)+(7*5)+(6*4)+(5*7)+(4*4)+(3*3)+(2*9)+(1*4)=158
158 % 10 = 8
So 1154743-94-8 is a valid CAS Registry Number.

1154743-94-8Downstream Products

1154743-94-8Relevant articles and documents

Convenient chemoenzymatic route to optically active β-aryl-δ-iodo-γ-lactones and β-aryl-γ-iodo-δ-lactones with the defined configurations of stereogenic centers

Gladkowski, Witold,Skrobiszewski, Andrzej,Mazur, Marcelina,Siepka, Monika,Bialoska, Agata

, p. 605 - 615 (2015)

Two δ-iodo-γ-lactones and two γ-iodo-δ-lactones substituted at the (β-position with phenyl or 4-methylphenyl ring have been synthesized in both enantiomeric forms. The starting materials were enantiomerically enriched allyl alcohols with an (E)-4-phenylbu

Highly regio- and stereoselective addition of organolithium reagents to extended conjugate amides using (S,S)-(+)-pseudoephedrine as chiral auxiliary

Ocejo, Marta,Carrillo, Luisa,Badia, Dolores,Vicario, Jose L.,Fernandez, Naiara,Reyes, Efraim

supporting information; experimental part, p. 4404 - 4407 (2009/09/06)

(Chemical Equation Presented) The conjugate addition of organolithium reagents to polyunsaturated conjugate amides containing (S,S)-(+)- pseudoephedrine as chiral auxiliary has been studied in detail. The reaction proceeded with good 1,4-selectivity and e

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 1154743-94-8