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3,4',5-Trichloro-4-methoxybiphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74298-91-2

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74298-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74298-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,9 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74298-91:
(7*7)+(6*4)+(5*2)+(4*9)+(3*8)+(2*9)+(1*1)=162
162 % 10 = 2
So 74298-91-2 is a valid CAS Registry Number.

74298-91-2SDS

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 3,4',5-trichloro-4-methoxybiphenyl

1.2 Other means of identification

Product number -
Other names 3,4',5-Trichlor-4-methoxy-biphenyl

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:74298-91-2 SDS

74298-91-2Downstream Products

74298-91-2Relevant academic research and scientific papers

Synthesis of hydroxylated PCB metabolites with the Suzuki-coupling

Lehmler, Hans-Joachim,Robertson, Larry W.

, p. 1119 - 1127 (2007/10/03)

An improved synthesis of hydroxylated polychlorinated biphenyls (PCBs) which are structurally related to the major hydroxy PCB congeners identified in human plasma is described. The coupling of (chlorinated) aryl boronic acids with bromochloro anisoles using the standard conditions of the Suzuki coupling gave the desired hydroxylated PCB metabolites in good to excellent yields. The approach offers the advantage of high selectivity and good yields compared to conventional methods such as the Cadogan reaction and allows the use of less toxic starting materials.

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