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188815-30-7

3-FLUORO-5-(TRIFLUOROMETHYL)BENZALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 188815-30-7 Structure

  • Basic information

    1. Product Name: 3-FLUORO-5-(TRIFLUOROMETHYL)BENZALDEHYDE
    2. Synonyms: 3-FLUORO-5-(TRIFLUOROMETHYL)BENZALDEHYDE;alpha,alpha,alpha,5-Tetrafluoro-m-tolualdehyde;à,à,à,5-tetrafluoro-m-tolualdehyde;3-Fluoro-5-(trifluoromethyl)benzaldehyde 97%;3-Fluoro-5-(trifluoromethyl)benzaldehyde97%;5-Tetrafluoro-M-Tolualdehyde;3-Fluoro-5-formylbenzotrifluoride;3-Fluoro-5-formylbenzotrifluoride, alpha,alpha,alpha,5-Tetrafluoro-m-tolualdehyde
    3. CAS NO:188815-30-7
    4. Molecular Formula: C8H4F4O
    5. Molecular Weight: 192.11
    6. EINECS: -0
    7. Product Categories: Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;Aldehydes;C8;Carbonyl Compounds;Fluorine series
    8. Mol File: 188815-30-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 175 °C(lit.)
    3. Flash Point: 159 °F
    4. Appearance: /
    5. Density: 1.376 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 1.48mmHg at 25°C
    7. Refractive Index: n20/D 1.45(lit.)
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    9. Solubility: N/A
    10. Sensitive: Air Sensitive
    11. BRN: 9121754
    12. CAS DataBase Reference: 3-FLUORO-5-(TRIFLUOROMETHYL)BENZALDEHYDE(CAS DataBase Reference)
    13. NIST Chemistry Reference: 3-FLUORO-5-(TRIFLUOROMETHYL)BENZALDEHYDE(188815-30-7)
    14. EPA Substance Registry System: 3-FLUORO-5-(TRIFLUOROMETHYL)BENZALDEHYDE(188815-30-7)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. RIDADR: NA 1993 / PGIII
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: IRRITANT
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 188815-30-7(Hazardous Substances Data)

188815-30-7 Usage

Chemical Properties

Colorless transparent liquid

Check Digit Verification of cas no

The CAS Registry Mumber 188815-30-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,8,1 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 188815-30:
(8*1)+(7*8)+(6*8)+(5*8)+(4*1)+(3*5)+(2*3)+(1*0)=177
177 % 10 = 7
So 188815-30-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H4F4O/c9-7-2-5(4-13)1-6(3-7)8(10,11)12/h1-4H

188815-30-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail

  • Alfa Aesar

  • (B20385)  3-Fluoro-5-(trifluoromethyl)benzaldehyde, 97%   

  • 188815-30-7

  • 1g

  • 492.0CNY

  • Detail

  • Alfa Aesar

  • (B20385)  3-Fluoro-5-(trifluoromethyl)benzaldehyde, 97%   

  • 188815-30-7

  • 5g

  • 1636.0CNY

  • Detail

188815-30-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-FLUORO-5-(TRIFLUOROMETHYL)BENZALDEHYDE

1.2 Other means of identification

Product number -
Other names 3-Fluoro-5-formylbenzotrifluoride

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:188815-30-7 SDS

188815-30-7Upstream product

188815-30-7Relevant articles and documents

Elemental fluorine. Part 21. (1) direct fluorination of benzaldehyde derivatives

Chambers, Richard D.,Sandford, Graham,Trmcic, Jelena,Okazoe, Takashi

, p. 339 - 344 (2013/01/03)

Direct fluorination of a range of benzaldehyde derivatives gives mixtures of fluorobenzaldehyde and benzoyl fluoride products in ratios that depend upon the nature of the ring substituent Electron-withdrawing substituents give predominantly benzoyl fluoride derivatives, whereas electron-donating substituents lead to fluoroarene systems. Separation of ring-fluorinated products can be easily accomplished by esterification of the benzoyl fluoride side products. Scale-up of these processes to provide significant quantities of appropriate fluorobenzaldehyde systems has also been achieved using continuous flow techniques.

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