Welcome to LookChem.com Sign In|Join Free

CAS

  • or

872832-01-4

Benzoic acid, 4-methoxy-, (2E)-2,5-hexadienyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

872832-01-4 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 872832-01-4 Structure

  • Basic information

    1. Product Name: Benzoic acid, 4-methoxy-, (2E)-2,5-hexadienyl ester
    2. Synonyms:
    3. CAS NO:872832-01-4
    4. Molecular Formula: C14H16O3
    5. Molecular Weight: 232.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 872832-01-4.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: Benzoic acid, 4-methoxy-, (2E)-2,5-hexadienyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 4-methoxy-, (2E)-2,5-hexadienyl ester(872832-01-4)
    11. EPA Substance Registry System: Benzoic acid, 4-methoxy-, (2E)-2,5-hexadienyl ester(872832-01-4)

  • 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: 872832-01-4(Hazardous Substances Data)

872832-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 872832-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,8,3 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 872832-01:
(8*8)+(7*7)+(6*2)+(5*8)+(4*3)+(3*2)+(2*0)+(1*1)=184
184 % 10 = 4
So 872832-01-4 is a valid CAS Registry Number.

872832-01-4Relevant articles and documents

Asymmetric total synthesis of the 1-epi-aglycon of the cripowellins A and B

Enders, Dieter,Lenzen, Achim,Backes, Michael,Janeck, Carsten,Catlin, Kelly,Lannou, Marie-Isabelle,Runsink, Jan,Raabe, Gerhard

, p. 10538 - 10551 (2005)

The unusual [5.3.2]-bicyclic structure of the insecticidal Amaryllidaceae alkaloids cripowellin A (1) and B (2) has been synthesized for the first time via a sequence of Sharpless dihydroxylation, ring-closing metathesis, and intramolecular Heck reaction. The asymmetric synthesis of the 1-epi-aglycon 82 proceeds with virtually complete diastereo- and enantioselectivity (de, ee ≥ 98%) in 13 steps and an overall yield of 5.6%. In addition, three alternative approaches toward the aglycon 3 are also described focusing on (1) the alkylation of the 2-benzazepinedithianes 35 and 36 with the electrophile 11, (2) a radical cyclization of the precursor (R/S,S,S)-39, and (3) an intramolecular arylation reaction of the aryl ketone 47.

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 872832-01-4