Welcome to LookChem.com Sign In|Join Free
  • or
(+)-Heptadeca-2t,8t,10t-triene-4,6-diyne-1,14-diol is a complex organic compound characterized by its unique molecular structure. It consists of a 17-carbon chain with three triple bonds (dienynes) at positions 2, 8, and 10, and two hydroxyl groups (diols) at positions 1 and 14. The compound exhibits a trans, trans, trans (t,t,t) configuration, indicating that the triple bonds are arranged in a specific geometric pattern. This molecule is chiral, meaning it has a non-superimposable mirror image, and the "(+)" notation signifies that it is the enantiomer that rotates plane-polarized light in a clockwise direction. The compound's structure and properties make it a potential candidate for various applications in chemistry and materials science, such as in the synthesis of pharmaceuticals or as a building block for more complex molecules.

463-02-5

Post Buying Request

463-02-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

463-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 463-02-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 463-02:
(5*4)+(4*6)+(3*3)+(2*0)+(1*2)=55
55 % 10 = 5
So 463-02-5 is a valid CAS Registry Number.

463-02-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name oenanthotoxin

1.2 Other means of identification

Product number -
Other names (2E,8E,10E)-2,8,10-heptadecatrien-4,6-diyne-1,14-diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:463-02-5 SDS

463-02-5Relevant academic research and scientific papers

Chemoenzymatic synthesis and cytotoxicity of oenanthotoxin and analogues

Sommerwerk, Sven,Heller, Lucie,Siewert, Bianka,Csuk, René

, p. 5595 - 5602 (2015)

We developed a synthetic scheme for the synthesis of naturally occurring (14R)-oenanthotoxin and several analogs. Key-steps of this synthesis were an efficient homo-coupling of alkynes and a chemoenzymatic resolution of racemic oenanthotoxin using novozyme 435 and vinyl acetate. The compounds were screened for their cytotoxic activity using a photometric sulforhodamine B assays and several human tumor cell lines. Oenanthotoxin and many derivatives thereof were cytotoxic to tumor cell lines as well as to non-malignant mouse fibroblasts. The highest activity was determined for human ovarian cancer cells A2780 with EC50 = 3.8 μM.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 463-02-5