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130506-22-8

6-NITROSO-1,2-BENZOPYRONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130506-22-8 Structure

  • Basic information

    1. Product Name: 6-NITROSO-1,2-BENZOPYRONE
    2. Synonyms: 6-NITROSO-1,2-BENZOPYRONE;6-Nitroso-2H-chroMen-2-one
    3. CAS NO:130506-22-8
    4. Molecular Formula: C9H5NO3
    5. Molecular Weight: 175.14
    6. EINECS: N/A
    7. Product Categories: ADP ribosyltransferase;A to;Enzyme Inhibitors by Enzyme
    8. Mol File: 130506-22-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 391.5°Cat760mmHg
    3. Flash Point: 221.1°C
    4. Appearance: /
    5. Density: 1.38g/cm3
    6. Vapor Pressure: 2.45E-06mmHg at 25°C
    7. Refractive Index: 1.633
    8. Storage Temp.: −20°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 6-NITROSO-1,2-BENZOPYRONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-NITROSO-1,2-BENZOPYRONE(130506-22-8)
    12. EPA Substance Registry System: 6-NITROSO-1,2-BENZOPYRONE(130506-22-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 130506-22-8(Hazardous Substances Data)

130506-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130506-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,0 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 130506-22:
(8*1)+(7*3)+(6*0)+(5*5)+(4*0)+(3*6)+(2*2)+(1*2)=78
78 % 10 = 8
So 130506-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H5NO3/c11-9-4-1-6-5-7(10-12)2-3-8(6)13-9/h1-5H

130506-22-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Nitroso-1,2-benzopyrone

1.2 Other means of identification

Product number -
Other names 6-nitrosochromen-2-one

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:130506-22-8 SDS

130506-22-8Downstream Products

130506-22-8Relevant articles and documents

Synergistic compositions useful as anti-tumor agents

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, (2008/06/13)

The subject invention provides for novel synergistic compositions useful for inactivating viruses or inducing apoptosis in tumor cells and for treating cancer or retroviral infections. Generally, the compositions comprise one or a plurality of ligands tha

Specific inactivators of "retroviral" (asymmetric) zinc fingers

-

, (2008/06/13)

The subject invention provides for novel compounds for inactivating viruses. These compounds include 6-nitroso-1,2-benzopyrone, 3-nitrosobenzamide, 5-nitroso-1(2H)isoquinolinone, 7-nitroso-1(2H)-isoquinolinone, 8-nitroso-1(2H)-isoquinolinone. The inventio

Adenosine diphosphoribose polymerase binding nitroso aromatic compounds useful as retroviral inactivating agents, anti-retroviral agents and anti-tumor agents

-

, (2008/06/13)

The subject invention provides for novel compounds for inactivating viruses. These compounds include 6-nitroso-1,2-benzopyrone, 3-nitrosobenzamide, 5-nitroso-1(2H)-isoquinolinone, 7-nitroso-1(2H)isoquinolinone, 8-nitroso-1(2H)isoquinolinone. The invention

Adenosine diphosphoribose polymerase binding nitroso aromatic compounds useful as retroviral inactivating agents, anti-retroviral agents and anti-tumor agents-54

-

, (2008/06/13)

The subject invention provides for novel compounds for inactivating viruses. These compounds include 6-nitroso-1,2-benzopyrone, 3-nitrosobenzamide, 5-nitroso-1(2H)-isoquinolinone, 7-nitroso-1(2H)-isoquinolinone, 8-nitroso-1(2H)-isoquinolinone. The inventi

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