Welcome to LookChem.com Sign In|Join Free
  • or
1,2,3,4-Tetrahydro-10-hydroxy-2-methyl-8-pentyl-5H-[1]benzopyrano[4,3-c]pyridin-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10344-38-4

Post Buying Request

10344-38-4 Suppliers

Recommended suppliers

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

10344-38-4 Usage

Molecular structure

A complex structure belonging to the class of benzopyranopyridinones and is a derivative of 5H-[1]benzopyrano[4,3-c]pyridin-5-one.

Functional groups

Contains a hydroxy group (-OH), a methyl group (-CH3), and a pentyl group (C5H11), which contribute to its molecular complexity.

Biological and pharmacological activities

Due to its intricate structure, it has potential biological and pharmacological activities, making it a subject of interest for further research in drug discovery and development.

Chemical class

It is a part of the benzopyranopyridinone class of compounds, which are known for their diverse range of biological activities.

Potential applications

Given its potential biological and pharmacological activities, 1,2,3,4-Tetrahydro-10-hydroxy-2-methyl-8-pentyl-5H-[1]benzopyrano[4,3-c]pyridin-5-one may be useful in the development of new drugs or therapies for various medical conditions.

Research interest

The compound's complex structure and potential activities make it a valuable target for further research in the fields of chemistry, biology, and pharmacology.

Synthesis

The synthesis of 1,2,3,4-Tetrahydro-10-hydroxy-2-methyl-8-pentyl-5H-[1]benzopyrano[4,3-c]pyridin-5-one may involve multiple steps and require specific reagents and conditions to form the desired molecular structure.

Structural analysis

Techniques such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, and X-ray crystallography can be used to analyze and confirm the structure of 1,2,3,4-Tetrahydro-10-hydroxy-2-methyl-8-pentyl-5H-[1]benzopyrano[4,3-c]pyridin-5-one.

Stability

The stability of 1,2,3,4-Tetrahydro-10-hydroxy-2-methyl-8-pentyl-5H-[1]benzopyrano[4,3-c]pyridin-5-one under various conditions (e.g., temperature, pH, light exposure) may be an important factor to consider for its potential applications.

Solubility

Understanding the solubility of 1,2,3,4-Tetrahydro-10-hydroxy-2-methyl-8-pentyl-5H-[1]benzopyrano[4,3-c]pyridin-5-one in different solvents can help in determining its suitability for various applications, such as drug formulation and delivery.

Check Digit Verification of cas no

The CAS Registry Mumber 10344-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,4 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10344-38:
(7*1)+(6*0)+(5*3)+(4*4)+(3*4)+(2*3)+(1*8)=64
64 % 10 = 4
So 10344-38-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H23NO3/c1-3-4-5-6-12-9-15(20)17-14-11-19(2)8-7-13(14)18(21)22-16(17)10-12/h9-10,20H,3-8,11H2,1-2H3

10344-38-4SDS

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 10-hydroxy-2-methyl-8-pentyl-3,4-dihydro-1H-chromeno[4,3-c]pyridin-5-one

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:10344-38-4 SDS

10344-38-4Downstream Products

10344-38-4Relevant academic research and scientific papers

Drugs derived from cannabinoids. 1. Nitrogen analogs, benzopyranopyridines and benzopyranopyrroles

Pars,Granchelli,Razdan,Keller,Teiger,Rosenberg,Harris

, p. 445 - 454 (2007/10/05)

Various nitrogen analogs of Δ(6a,10a) tetrahydrocannabinol were synthesized by a general procedure described in an earlier communication. Minimum effective doses (MED(50's)) and lethal doses (LD(50's)) were determined by a modified Irwin mouse screen afte

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 10344-38-4