Welcome to LookChem.com Sign In|Join Free
  • or
Deethyaconitine is a potent alkaloid derived from the Aconitum plant, commonly known as monkshood. It is a naturally occurring toxic compound that belongs to the family of diterpenoid alkaloids. Deethyaconitine exhibits significant pharmacological properties, including local anesthetic, analgesic, and anti-inflammatory effects. However, due to its high toxicity, it can cause severe adverse effects such as paralysis, respiratory failure, and even death if ingested in large amounts. The compound has been studied for its potential therapeutic applications, but its use is limited by its narrow therapeutic index and the risk of serious side effects.

3327-35-3

Post Buying Request

3327-35-3 Suppliers

Recommended suppliers

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

3327-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3327-35-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3327-35:
(6*3)+(5*3)+(4*2)+(3*7)+(2*3)+(1*5)=73
73 % 10 = 3
So 3327-35-3 is a valid CAS Registry Number.

3327-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-desethylaconitine

1.2 Other means of identification

Product number -
Other names N-deethylaconitine

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:3327-35-3 SDS

3327-35-3Relevant academic research and scientific papers

Oxidation of aconitine by potassium permanganate. A new N-de-ethyl-7,17-secoimino derivative

Sultankhodzhaev

, p. 844 - 845 (2009)

The alkaloid aconitine was oxidized by potassium permanganate in aqueous acetone. It was shown that the oxidation formed three products including the previously described N-de-ethylaconitine, N-de-ethyl-19-oxoaconitine, and a new N-de-ethyl-7,17-secoimino

DEOXYGENATION REACTIONS OF C19-DITERPENOID ALKALOIDS

Kulanthaivel, Palaniappan,Pelletier, S. William

, p. 4313 - 4320 (2007/10/02)

Efficient methods for deoxygenation of secondary and tertiary alcohols of some C19-diterpenoid alkaloids are presented.Delphisine (12) was converted to 1-deoxydelphisine (19) via either 1,2-pyrodelphisine (17) or phenyl thionocarbonate 20.The following alkaloids were deoxygenated via their thiocarbonylimidazolyl derivatives: 14-acetyldelcosine (13) to 14-acetyl-1-deoxydelcosine (22); alkaline hydrolysis of 22 gave 1-deoxydelcosine (23); aconitine (24) to 3-deoxyaconitine (27); yunaconitine (25) to crassicauline A (28).Deoxygenation of 14-acetyldictyocarpine (30) via the chloro-derivate 31 gave 14-acetyl-10-deoxydictiocarpine (34).Reduction of 31 with LiAlH4 gave the unusual elimination product 32.An improved partial synthesis of hypaconitine (35) from aconitine (24) is also presented.

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 3327-35-3