Welcome to LookChem.com Sign In|Join Free
  • or
(2E)-2-[1-(pyridin-2-yl)ethylidene]-N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)hydrazinecarbothioamide is a complex chemical compound that features a pyridine group, a tricyclo[3.3.1.1~3,7~]dec-1-yl group, and a hydrazinecarbothioamide group. As a hydrazine derivative, (2E)-2-[1-(pyridin-2-yl)ethylidene]-N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)hydrazinecarbothioamide is characterized by the presence of a double bond, denoted by the (2E)-2 notation. Its intricate molecular structure suggests potential applications in research and development or pharmaceuticals, given the bioactive nature of the hydrazinecarbothioamide group.

70618-55-2

Post Buying Request

70618-55-2 Suppliers

Recommended suppliers

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

70618-55-2 Usage

Uses

Used in Pharmaceutical Research and Development:
(2E)-2-[1-(pyridin-2-yl)ethylidene]-N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)hydrazinecarbothioamide is used as a research compound for exploring its potential pharmaceutical applications. The presence of the hydrazinecarbothioamide group indicates that it may possess bioactive properties, making it a candidate for further investigation into its effects on biological systems.
Used in Chemical Synthesis:
In the chemical synthesis industry, (2E)-2-[1-(pyridin-2-yl)ethylidene]-N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)hydrazinecarbothioamide may be utilized as a precursor or intermediate in the production of other complex organic compounds. Its unique structure could be valuable for creating novel molecules with specific properties or functions.
Used in Medicinal Chemistry:
(2E)-2-[1-(pyridin-2-yl)ethylidene]-N-(tricyclo[3.3.1.1~3,7~]dec-1-yl)hydrazinecarbothioamide is used as a lead compound in medicinal chemistry for the development of new drugs. Its complex structure and the presence of bioactive groups suggest that it could be optimized to target specific biological pathways or receptors, potentially leading to the discovery of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 70618-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,1 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70618-55:
(7*7)+(6*0)+(5*6)+(4*1)+(3*8)+(2*5)+(1*5)=122
122 % 10 = 2
So 70618-55-2 is a valid CAS Registry Number.

70618-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-adamantyl)-3-[(E)-1-pyridin-2-ylethylideneamino]thiourea

1.2 Other means of identification

Product number -
Other names -

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:70618-55-2 SDS

70618-55-2Upstream product

70618-55-2Downstream Products

70618-55-2Relevant academic research and scientific papers

ADAMANTANE COMPOUNDS

-

Page/Page column 41; 44; 46, (2018/01/20)

The present invention relates to new multi-functional compounds that are useful in the treatment of neurodegenerative diseases, such as Alzheimer's disease, to the preparation of the compounds, and to compositions including the compounds. The present invention also relates to the use of the compounds, as well as compositions including the compounds, in treating or preventing neurodegenerative diseases.

2-Acetylpyridine thiosemicarbazones. 1. A new class of potential antimalarial agents

Klayman,Bartosevich,Griffin,Mason,Scovill

, p. 855 - 862 (2007/10/04)

Based on the antimalarial properties observed for 2-acetylpyridine 4-phenyl-3-thiosemicarbazone (1), an extensive series of related thiosemicarbazones was prepared and tested against Plasmodium berghei in mice. Screening results indicated that the presence of the 2-pyridylethylidene group was critical and that certain phenyl, benzyl, phenethyl, or cycloalkyl groups at N4 of the thiosemicarbazone moiety also contribute to antimalarial activity.

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 70618-55-2