Welcome to LookChem.com Sign In|Join Free

CAS

  • or

27575-78-6

Post Buying Request

27575-78-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

27575-78-6 Usage

Description

1-[bis(4-chlorophenyl)methyl]-4-chloro-benzene, also known as Tris(4-chlorophenyl)methane, is an organic compound with the molecular formula C19H13Cl3. It is characterized by its chlorinated aromatic structure, which consists of a central benzene ring with a tris(4-chlorophenyl)methyl group attached to it. 1-[bis(4-chlorophenyl)methyl]-4-chloro-benzene is known for its stability and is commonly used as a standard in various analytical and environmental applications.

Uses

1. Used in Environmental Testing and Research:
Tris(4-chlorophenyl)methane is used as a standard compound for environmental testing and research purposes. It aids in the study of the geographical distribution, accumulation kinetics, and health risks associated with organochlorines in human breast milk from different regions, such as Indonesia.
2. Used in Analytical Chemistry for Sample Preparation:
In the field of analytical chemistry, Tris(4-chlorophenyl)methane is employed as a reference material for the development and optimization of extraction and cleanup methods. These methods are crucial for the accurate analysis of phenolic and neutral organohalogens in plasma samples, which are essential for understanding the presence and impact of these compounds on human health and the environment.
3. Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, Tris(4-chlorophenyl)methane, due to its structural properties, could potentially be used in the pharmaceutical industry as a starting material or intermediate for the synthesis of various drugs, particularly those targeting the central nervous system or other organ systems where chlorinated aromatic compounds are known to have biological activity.
4. Used in Chemical Research and Development:
Tris(4-chlorophenyl)methane can also be utilized in chemical research and development for the synthesis of novel compounds with potential applications in various industries, such as agrochemicals, materials science, and specialty chemicals. Its unique structure and reactivity make it a valuable tool for exploring new chemical reactions and developing innovative products.

Check Digit Verification of cas no

The CAS Registry Mumber 27575-78-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,5,7 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27575-78:
(7*2)+(6*7)+(5*5)+(4*7)+(3*5)+(2*7)+(1*8)=146
146 % 10 = 6
So 27575-78-6 is a valid CAS Registry Number.

27575-78-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[bis(4-chlorophenyl)methyl]-4-chlorobenzene

1.2 Other means of identification

Product number -
Other names 4,4',4''-trichlorotriphenylmethane

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:27575-78-6 SDS

27575-78-6Relevant articles and documents

Benzylic Phosphates in Friedel-Crafts Reactions with Activated and Unactivated Arenes: Access to Polyarylated Alkanes

Pallikonda, Gangaram,Chakravarty, Manab

, p. 2135 - 2142 (2016/03/15)

Easily reachable electron-poor/rich primary and secondary benzylic phosphates are suitably used as substrates for Friedel-Crafts benzylation reactions with only 1.2 equiv activated/deactivated arenes (no additional solvent) to access structurally and electronically diverse polyarylated alkanes with excellent yields and selectivities at room temperature. Specifically, diversely substituted di/triarylmethanes are generated within 2-30 min using this approach. A wide number of electron-poor polyarylated alkanes are easily accomplished through this route by just tuning the phosphates.

DDT, a potentiaal source of environmental tris(4-chlorophenyl)methane and tris(4-chlorophenyl) methanol

Buser

, p. 2133 - 2139 (2007/10/03)

-

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 27575-78-6