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2-FLUORO-3'-METHOXYBENZOPHENONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 890098-08-5 Structure
  • Basic information

    1. Product Name: 2-FLUORO-3'-METHOXYBENZOPHENONE
    2. Synonyms: 2-FLUORO-3'-METHOXYBENZOPHENONE;(2-fluorophenyl)-(3-methoxyphenyl)methanone
    3. CAS NO:890098-08-5
    4. Molecular Formula: C14H11FO2
    5. Molecular Weight: 230.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 890098-08-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 366.4°C at 760 mmHg
    3. Flash Point: 169.4°C
    4. Appearance: /
    5. Density: 1.176g/cm3
    6. Vapor Pressure: 1.47E-05mmHg at 25°C
    7. Refractive Index: 1.553
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-FLUORO-3'-METHOXYBENZOPHENONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-FLUORO-3'-METHOXYBENZOPHENONE(890098-08-5)
    12. EPA Substance Registry System: 2-FLUORO-3'-METHOXYBENZOPHENONE(890098-08-5)
  • 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: 890098-08-5(Hazardous Substances Data)

890098-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 890098-08-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,0,0,9 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 890098-08:
(8*8)+(7*9)+(6*0)+(5*0)+(4*9)+(3*8)+(2*0)+(1*8)=195
195 % 10 = 5
So 890098-08-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H11FO2/c1-17-11-6-4-5-10(9-11)14(16)12-7-2-3-8-13(12)15/h2-9H,1H3

890098-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-fluorophenyl)-(3-methoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names 2-FLUORO-3'-METHOXYBENZOPHENONE

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:890098-08-5 SDS

890098-08-5Downstream Products

890098-08-5Relevant articles and documents

Preparation of Functionalized Diorganomagnesium Reagents in Toluene via Bromine or Iodine/Magnesium-Exchange Reactions

Desaintjean, Alexandre,Danton, Fanny,Knochel, Paul

supporting information, p. 4461 - 4476 (2021/08/13)

A wide range of polyfunctionalized di(hetero)aryl- and dialkenyl-magnesium reagents are prepared in toluene within 10 to 120 minutes between 78 C and 25 C via an I/Mg- or Br/Mg-exchange reaction using reagents of the general formula R2Mg (R = sBu, Mes). Highly sensitive functional groups, such as triazene or nitro, are tolerated in these exchange reactions, enabling the synthesis of various functionalized (hetero)arene and alkene derivatives after quenching with several electrophiles including allyl bromides, acyl chlorides, aldehydes, ketones, and aryl iodides.

Elemental step thermodynamics of various analogues of indazolium alkaloids to obtaining hydride in acetonitrile

Lei, Nan-Ping,Fu, Yan-Hua,Zhu, Xiao-Qing

, p. 11472 - 11485 (2015/12/04)

A series of analogues of indazolium alkaloids were designed and synthesized. The thermodynamic driving forces of the 6 elemental steps for the analogues of indazolium alkaloids to obtain hydride in acetonitrile were determined using an isothermal titration calorimeter (ITC) and electrochemical methods, respectively. The effects of molecular structure and substituents on the thermodynamic driving forces of the 6 steps were examined. Meanwhile, the oxidation mechanism of NADH coenzyme by indazolium alkaloids was examined using the chemical mimic method. The result shows that the oxidation of NADH coenzyme by indazolium alkaloids in vivo takes place by one-step concerted hydride transfer mechanism.

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