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(7S)-7-METHYL-5-(4-NITROPHENYL)-7,8-DIHYDRO-5H-[1,3]DIOXOLO[4,5-G]ISOCHROMENE is a chemical compound with the molecular formula C16H11NO6. It belongs to the class of organic compounds known as flavonoids and is a derivative of chromene, characterized by the presence of a nitrophenyl group. (7S)-7-METHYL-5-(4-NITROPHENYL)-7,8-DIHYDRO-5H-[1,3]DIOXOLO[4,5-G]ISOCHROMENE has potential biological activities and may have applications in the fields of medicine and pharmaceuticals. Its unique structure and properties also make it an interesting target for further research and development.

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  • (7S)-7-METHYL-5-(4-NITROPHENYL)-7,8-DIHYDRO-5H-[1,3]DIOXOLO[4,5-G]ISOCHROMENE

    Cas No: 196303-01-2

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  • 196303-01-2 Structure
  • Basic information

    1. Product Name: (7S)-7-METHYL-5-(4-NITROPHENYL)-7,8-DIHYDRO-5H-[1,3]DIOXOLO[4,5-G]ISOCHROMENE
    2. Synonyms: (7S)-7-METHYL-5-(4-NITROPHENYL)-7,8-DIHYDRO-5H-[1,3]DIOXOLO[4,5-G]ISOCHROMENE
    3. CAS NO:196303-01-2
    4. Molecular Formula: C17H15NO5
    5. Molecular Weight: 313.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 196303-01-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (7S)-7-METHYL-5-(4-NITROPHENYL)-7,8-DIHYDRO-5H-[1,3]DIOXOLO[4,5-G]ISOCHROMENE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (7S)-7-METHYL-5-(4-NITROPHENYL)-7,8-DIHYDRO-5H-[1,3]DIOXOLO[4,5-G]ISOCHROMENE(196303-01-2)
    11. EPA Substance Registry System: (7S)-7-METHYL-5-(4-NITROPHENYL)-7,8-DIHYDRO-5H-[1,3]DIOXOLO[4,5-G]ISOCHROMENE(196303-01-2)
  • 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: 196303-01-2(Hazardous Substances Data)

196303-01-2 Usage

Uses

Used in Pharmaceutical Industry:
(7S)-7-METHYL-5-(4-NITROPHENYL)-7,8-DIHYDRO-5H-[1,3]DIOXOLO[4,5-G]ISOCHROMENE is used as a potential therapeutic agent for various medical conditions due to its potential biological activities.
Used in Research and Development:
In the field of scientific research, (7S)-7-METHYL-5-(4-NITROPHENYL)-7,8-DIHYDRO-5H-[1,3]DIOXOLO[4,5-G]ISOCHROMENE serves as a subject of study for understanding its structure, properties, and potential applications in medicine and pharmaceuticals.
Used in Drug Design and Synthesis:
(7S)-7-METHYL-5-(4-NITROPHENYL)-7,8-DIHYDRO-5H-[1,3]DIOXOLO[4,5-G]ISOCHROMENE can be utilized as a starting material or a structural motif in the design and synthesis of new drugs, taking advantage of its unique chemical properties and potential biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 196303-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,3,0 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 196303-01:
(8*1)+(7*9)+(6*6)+(5*3)+(4*0)+(3*3)+(2*0)+(1*1)=132
132 % 10 = 2
So 196303-01-2 is a valid CAS Registry Number.

196303-01-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (7S)-7-methyl-5-(4-nitrophenyl)-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isochromene

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:196303-01-2 SDS

196303-01-2Relevant articles and documents

Sassafras oil, carrot bits and microwaves: Green lessons learned from the formal total synthesis of (-)-talampanel

Omori, Alvaro Takeo,De Oliveira, Camila De Souza,Andrade, Kleber Tellini,Capeletto, Marina Gon?alves

, p. 103563 - 103565 (2015/12/23)

A formal total synthesis of (-)-talampanel (1), a 2,3-benzodiazepine is described. This work was undertaken to utilize greener reaction conditions. Safrole (a renewable source) was converted to (1) in eight steps, including an enantioselective bioreduction using carrots as the key step. Microwave irradiation was also used to perform three reaction steps.

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