Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bisis a chemical compound that is commonly used as an intermediate or starting material in the synthesis of various organic compounds. It is a derivative of benzoyl chloride, and the addition of the 2,2,2-trifluoro-1-(trifluoromethyl)ethylidene group makes it a highly reactive and versatile compound. This chemical is utilized in the pharmaceutical, agrochemical, and manufacturing industries for the production of various organic compounds, including pharmaceuticals, pesticides, and polymers. Due to its reactivity and versatility, it is an important chemical in the field of organic synthesis.

1102-92-7 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1102-92-7 Structure
  • Basic information

    1. Product Name: Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-
    2. Synonyms: Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-
    3. CAS NO:1102-92-7
    4. Molecular Formula: C17H8Cl2F6O2
    5. Molecular Weight: 429
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1102-92-7.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: Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-(1102-92-7)
    11. EPA Substance Registry System: Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-(1102-92-7)
  • 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: 1102-92-7(Hazardous Substances Data)

1102-92-7 Usage

Uses

Used in Pharmaceutical Industry:
Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bisis used as a key intermediate in the synthesis of various pharmaceutical compounds. Its high reactivity and versatility make it an essential component in the production of drugs with diverse therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bisis used as a starting material for the synthesis of various pesticides. Its unique properties allow for the development of effective and targeted pest control solutions.
Used in Manufacturing Industry:
Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bisis also used in the manufacturing industry for the production of various polymers and other organic compounds. Its reactivity and versatility contribute to the development of innovative materials with a wide range of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1102-92-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,0 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1102-92:
(6*1)+(5*1)+(4*0)+(3*2)+(2*9)+(1*2)=37
37 % 10 = 7
So 1102-92-7 is a valid CAS Registry Number.

1102-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(4-carbonochloridoylphenyl)-1,1,1,3,3,3-hexafluoropropan-2-yl]benzoyl chloride

1.2 Other means of identification

Product number -
Other names 4,4'-(hexafluoroisopropylidene)bis(benzoyl chloride)

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:1102-92-7 SDS

1102-92-7Relevant articles and documents

Preparation and properties of polybenzoxazole-based gas separation membranes: A comparative study between thermal rearrangement (TR) of poly(hydroxyimide) and thermal cyclodehydration of poly(hydroxyamide)

Kushwaha, Ashish,Dose, Michelle E.,Smith, Zachary P.,Luo, Shuangjiang,Freeman, Benny D.,Guo, Ruilan

, p. 81 - 93 (2015)

This comparative study focuses on the cyclodehydration reaction of poly(hydroxyamide)s (PHAs) and the thermal rearrangement (TR) reaction of aromatic poly(hydroxyimide)s (APIs) to produce polybenzoxazoles (PBOs) for application as gas separation membranes

Novel synthetic method for 2,2-bis(4-aminophenyl)hexafluoropropane

-

, (2018/09/08)

The invention relates to a novel synthetic method for 2,2-bis(4-aminophenyl)hexafluoropropane. The novel synthetic method is mainly to solve problems like high hazards, large product separation and purification difficulties, expensive raw materials and harsh reaction conditions in a traditional synthetic method. The method comprises the following steps: with 2,2-bis(4-methylphenyl)hexafluoropropane as a raw material, oxidizing the 2,2-bis(4-methylphenyl)hexafluoropropane into 2,2-bis(4-carboxylphenyl)hexafluoropropane through chromium trioxide, then carrying out an acyl chlorination reaction,introducing ammonia gas, carrying out an amidation reaction so as to obtain 2,2-bis(4-formamidophenyl)hexafluoropropane, and carrying out a Hoffman reaction in a sodium hypochlorite solution so as toobtain a target product. The method provided by the invention has the advantages of cheap and easily-available raw materials, mild reaction conditions, easy industrialization, etc.

Radical-forming polyamides for self-decontamination coatings

Damaceanu, Mariana-Dana,Rusu, Radu-Dan,Bruma, Maria

, p. 799 - 806 (2013/05/09)

Design and synthesis of thermally stable polyamides with improved solubility based on an asymmetrical aromatic diamine containing phenoxy substituted benzophenone segment was the main objective of this work. These polymers were easily soluble at room temperature in polar aprotic solvents and even in less polar solvents, such as tetrahydrofuran. The polymers showed excellent thermal stability, up to 385°C, and exhibited glass transition in the range of 225-256°C. All the polymers emitted an intense blue light upon irradiation with UV light, due to the emission from the benzophenone chromophore. The free-standing films having the thickness in the range of tens of micrometers obtained from these polymers were flexible, tough, and maintained their integrity after repeated bendings. To investigate the radical-forming ability of the polyamides for decomposing surrounding harmful materials, degradation of methylene blue by the polymer films was studied.

Blue fluorescent polyamides containing naphthalene and oxadiazole rings

Damaceanu, Mariana-Dana,Rusu, Radu-Dan,Nicolescu, Alina,Bruma, Maria

body text, p. 893 - 906 (2012/01/12)

New polyamides containing 1,3,4-oxadiazole and naphthalene rings were prepared by low-temperature solution polycondensation reaction of a new diamine containing preformed oxadiazole ring with various aromatic diacid chlorides. Elemental analysis, mass, infrared, and nuclear magnetic resonance spectroscopy were used to confirm the structure of the monomers and corresponding polymers. The thermal stability and glass transition temperatures of these poly(oxadiazole-amide)s were measured and compared with those of related polymers. Their good solubility allows them to be processed in very thin films with smooth surfaces, without pinholes or cracks, when studied by atomic force microscopy. Upon irradiation with UV light the polymers showed photoluminescence maxima in the blue spectral range, both in solution and in solid state. Cyclic voltammetry (CV) was performed in order to obtain information about the electrochemical stability and reversibility of the redox processes of these polyamides. The highest occupied molecular orbital and the lowest unoccupied molecular orbital energy levels, and electrochemical and optical band gap values were calculated by using the results of CV and UV/vis, respectively, showing very good electron and hole injection and transport characteristics. These properties make the present polymers suitable for application in electroluminescent devices.

Study of fluorinated poly(1,3,4-oxadiazole-amide)s

Dǎmǎceanu, Mariana-Dana,Brumǎ, Maria

, p. 815 - 830 (2007/10/03)

Three aromatic fluorinated poly(1,3,4-oxadiazole-amide) were synthesized by solution polycondensation reaction of aromatic diamines containing preformed 1,3,4-oxadiazole ring with a diacid chloride incorporating hexafluorisopropylidene unit. All polymers

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1102-92-7