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1,1'-Biphenyl, 4-[(octyloxy)phenylmethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

693272-43-4

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693272-43-4 Usage

Chemical structure

A biphenyl core with a phenylmethyl group attached to the fourth position of one benzene ring, and an octyloxy group attached to the fourth position of the other benzene ring.

Molecular weight

Approximately 374.54 g/mol (calculated from the molecular formula)

Functional groups

Phenyl, phenylmethyl, and octyloxy groups

Applications

Building block in the synthesis of liquid crystals, polymers, and other organic materials

Industrial uses

Electronic devices, pharmaceuticals, and advanced materials

Thermal stability

High thermal stability, making it suitable for various industrial processes and manufacturing applications

Solubility

Soluble in organic solvents, which is desirable for chemical reactions and processing

Physical state

Likely a solid at room temperature, based on its molecular weight and structure

Optical properties

Potential for anisotropic properties due to its molecular structure, which could be useful in liquid crystal applications

Chemical reactivity

May undergo reactions such as electrophilic aromatic substitution, nucleophilic aromatic substitution, and oxidation, depending on the specific reaction conditions and reagents used

Hazards

Potential hazards may include flammability, toxicity, or reactivity with other chemicals, depending on the specific properties of the compound and the conditions under which it is used

Storage and handling

Should be stored in a cool, dry, and well-ventilated area, away from incompatible substances, and handled with appropriate safety measures, such as wearing gloves and using eye protection

Regulatory information

Depending on the specific jurisdiction and intended use, 1,1'-Biphenyl, 4-[(octyloxy)phenylmethyl]- may be subject to various regulations, such as those related to chemical safety, environmental protection, and worker protection

Synthesis

The compound can be synthesized through various methods, such as the reaction of a biphenyl derivative with an appropriate phenylmethyl and octyloxy group-containing reagents, followed by functional group transformations and purification steps.

Check Digit Verification of cas no

The CAS Registry Mumber 693272-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,3,2,7 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 693272-43:
(8*6)+(7*9)+(6*3)+(5*2)+(4*7)+(3*2)+(2*4)+(1*3)=184
184 % 10 = 4
So 693272-43-4 is a valid CAS Registry Number.

693272-43-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-((octyloxy)(phenyl)methyl)-1,1'-biphenyl

1.2 Other means of identification

Product number -
Other names -

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:693272-43-4 SDS

693272-43-4Downstream Products

693272-43-4Relevant academic research and scientific papers

p-Methoxy Diphenylmethanol (MDPM), p-Phenyl Diphenylmethanol (PDPM), and p-Phenylphenyl Diphenylmethanol (PPDPM) - Protecting Groups for Alcohols - Protection and Deprotection

Sharma,Prasad, T. Rajendra,Srinivas, Rakesh B.

, p. 941 - 950 (2007/10/03)

Two new protecting groups viz. p-phenyl diphenylmethanol (PDPM) and p-phenylphenyl diphenylmethanol (PPDPM) were prepared and utilized along with p-methoxy diphenylmethanol (MDPM), for the protection of alcohols in the presence of Yb(OTf)3. Deprotection of the above ethers was achieved using DDQ or CF3COOH.

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