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6-Nitroisoquinoline, an organic compound with the molecular formula C9H6N2O2, is a nitro-substituted derivative of isoquinoline. It features a quinoline ring with a nitro group attached at the 6-position, giving it a yellow solid appearance. With a melting point of 126-128°C, it is sparingly soluble in water and is classified as a hazardous substance, necessitating controlled handling and use with proper safety measures.

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  • 70538-57-7 Structure
  • Basic information

    1. Product Name: 6-NITROISOQUINOLINE
    2. Synonyms: 6-NITROISOQUINOLINE
    3. CAS NO:70538-57-7
    4. Molecular Formula: C9H6N2O2
    5. Molecular Weight: 174.04
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 70538-57-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 353.325 °C at 760 mmHg
    3. Flash Point: 167.485 °C
    4. Appearance: /
    5. Density: 1.354 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-NITROISOQUINOLINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-NITROISOQUINOLINE(70538-57-7)
    11. EPA Substance Registry System: 6-NITROISOQUINOLINE(70538-57-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 70538-57-7(Hazardous Substances Data)

70538-57-7 Usage

Uses

Used in Pharmaceutical Industry:
6-Nitroisoquinoline is utilized as a key building block in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Dye Industry:
In the dye industry, 6-Nitroisoquinoline serves as a crucial intermediate for the production of dyes. Its chemical properties enable the creation of a wide range of colorants used in various applications, including textiles, plastics, and printing inks.
As a Hazardous Substance:
Due to its classification as a hazardous substance, 6-Nitroisoquinoline requires careful handling and use in a controlled environment. This ensures the safety of workers and minimizes potential environmental impacts during its production, storage, and application processes.

Check Digit Verification of cas no

The CAS Registry Mumber 70538-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,3 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70538-57:
(7*7)+(6*0)+(5*5)+(4*3)+(3*8)+(2*5)+(1*7)=127
127 % 10 = 7
So 70538-57-7 is a valid CAS Registry Number.

70538-57-7SDS

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 6-Nitroisoquinoline

1.2 Other means of identification

Product number -
Other names 6-NITROISOQUINOLINE

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:70538-57-7 SDS

70538-57-7Relevant articles and documents

Synthesis of Isoquinolines from Indenes

Miller, R. Bryan,Frincke, James M.

, p. 5312 - 5315 (2007/10/02)

A general procedure for the synthesis of isoquinolines from appropriately substituted indenes is described.Ozonolysis of the indenes followed by reductive workup gives intermediate homophthalaldehydes which are treated with ammonium hydroxide to give the isoquinolines.This "one-pot", three-step reaction sequence was applied to the formation of all of the mono-C-methyl-substituted isoquinolines in a regiospecific manner.The procedure is applicable to both electron-withdrawing and electron-donating substituents on the indene system.In this manner the 6- and 7-nitro-,-bromo-, and -iodoisoquinolines were prepared.

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