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1(2H)-Naphthalenone, 8-amino-5,6-difluoro-3,4-dihydro-4-hydroxy(9CI) is a synthetic chemical compound with the molecular formula C10H7F2NO2. It belongs to the class of naphthalenone derivatives and is characterized by its unique structure and potential medicinal properties. 1(2H)-Naphthalenone, 8-amino-5,6-difluoro-3,4-dihydro-4-hydroxy(9CI) is of significant interest in pharmaceutical research due to its promising candidacy for the development of new drugs and its potential applications in the field of medicinal chemistry.

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  • 1(2H)-Naphthalenone, 8-amino-5,6-difluoro-3,4-dihydro-4-hydroxy- (9CI)

    Cas No: 210346-35-3

  • USD $ 1.9-2.9 / Gram

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  • 210346-35-3 Structure
  • Basic information

    1. Product Name: 1(2H)-Naphthalenone, 8-amino-5,6-difluoro-3,4-dihydro-4-hydroxy- (9CI)
    2. Synonyms: 1(2H)-Naphthalenone, 8-amino-5,6-difluoro-3,4-dihydro-4-hydroxy- (9CI)
    3. CAS NO:210346-35-3
    4. Molecular Formula: C10H9F2NO2
    5. Molecular Weight: 213.1807664
    6. EINECS: N/A
    7. Product Categories: ALCOHOL
    8. Mol File: 210346-35-3.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: 1(2H)-Naphthalenone, 8-amino-5,6-difluoro-3,4-dihydro-4-hydroxy- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1(2H)-Naphthalenone, 8-amino-5,6-difluoro-3,4-dihydro-4-hydroxy- (9CI)(210346-35-3)
    11. EPA Substance Registry System: 1(2H)-Naphthalenone, 8-amino-5,6-difluoro-3,4-dihydro-4-hydroxy- (9CI)(210346-35-3)
  • 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: 210346-35-3(Hazardous Substances Data)

210346-35-3 Usage

Uses

Used in Pharmaceutical Research:
1(2H)-Naphthalenone, 8-amino-5,6-difluoro-3,4-dihydro-4-hydroxy(9CI) is used as an active ingredient in the development of new drugs. Its unique structure and properties make it a promising candidate for further investigation and study in the field of medicinal chemistry.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1(2H)-Naphthalenone, 8-amino-5,6-difluoro-3,4-dihydro-4-hydroxy(9CI) is utilized for its potential to contribute to the discovery and design of novel therapeutic agents. Its specific characteristics and synthetic nature allow researchers to explore its potential applications in creating effective treatments for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 210346-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,3,4 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 210346-35:
(8*2)+(7*1)+(6*0)+(5*3)+(4*4)+(3*6)+(2*3)+(1*5)=83
83 % 10 = 3
So 210346-35-3 is a valid CAS Registry Number.

210346-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-amino-5,6-difluoro-4-hydroxy-3,4-dihydro-2H-naphthalen-1-one

1.2 Other means of identification

Product number -
Other names 1(2h)-naphthalenone,8-amino-5,6-difluoro-3,4-dihydro-4-hydroxy

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:210346-35-3 SDS

210346-35-3Downstream Products

210346-35-3Relevant articles and documents

Synthesis and antitumor activity of ring A- and F-modified hexacyclic camptothecin analogues

Sugimori, Masamichi,Ejima, Akio,Ohsuki, Satoru,Uoto, Kouichi,Mitsui, Ikuo,Kawato, Yasuyoshi,Hirota, Yasuhide,Sato, Keiki,Terasawa, Hirofumi

, p. 2308 - 2318 (2007/10/03)

Nineteen ring A- and F-modified hexacyclic analogues of camptothecin were synthesized by Friedlander condensation of appropriately substituted bicyclic amino ketones with tricyclic ketone and were evaluated for cytotoxicity and topoisomerase I inhibitory

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