Welcome to LookChem.com Sign In|Join Free
  • or
Benzo[h]-1,6-naphthyridine is a heterocyclic aromatic compound with the chemical formula C13H9N. It is a derivative of naphthyridine, which is a fused ring system consisting of a benzene ring and a pyridine ring. Benzo[h]-1,6-naphthyridine is characterized by its tricyclic structure, with one nitrogen atom in the pyridine ring and another in the benzene ring. Benzo[h]-1,6-naphthyridine is an important building block in the synthesis of various pharmaceuticals and agrochemicals due to its unique electronic properties and potential for further functionalization. It is also known for its potential applications in materials science, such as in the development of new dyes and pigments. The compound's structure and properties make it a versatile intermediate in organic synthesis, allowing for the creation of a wide range of complex molecules with diverse applications.

230-51-3

Post Buying Request

230-51-3 Suppliers

Recommended suppliers

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

230-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 230-51-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,3 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 230-51:
(5*2)+(4*3)+(3*0)+(2*5)+(1*1)=33
33 % 10 = 3
So 230-51-3 is a valid CAS Registry Number.

230-51-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzo[h][1,6]naphthyridine

1.2 Other means of identification

Product number -
Other names 1,6-diazaphenanthrene

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:230-51-3 SDS

230-51-3Upstream product

230-51-3Relevant academic research and scientific papers

ν-triazolines. Part 40. Thermal and photochemical transformations of 1-biaryl-5-amino-4,5-dihydro-ν-triazoles: A new synthetic approach to 6-alkylphenanthridines and aza-analogs

Erba, Emanuela,Pocar, Donato,Trimarco, Pasqualina

, p. 3535 - 3539 (2007/10/03)

1-Biaryl-5-morpholino-ν-triazolines 4 were prepared from aliphatic aldehydes 1, morpholine and 2-azidobiaryls 3. They underwent smooth thermal rearrangement to tertiary amidines 5 which were photochemically cyclized to 6-alkylphenanthridines 6a,b,e,f and analogs 6c,d and 8a,b with morpholine elimination. Direct photolysis of triazolines 4 afforded lower yields of the same compounds 6 together with by-products indicative of the mechanism of the photochemical rearrangement which is discussed.

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 230-51-3