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151276-10-7

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151276-10-7 Usage

General Description

1,2-dichloro-4-(trifluoroMethoxy)benzene is a chemical compound with the molecular formula C8H5Cl2F3O. It is a colorless to pale yellow liquid with a faint, sweet odor. 1,2-dichloro-4-(trifluoroMethoxy)benzene is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used as a solvent in chemical reactions and as an intermediate in the production of other organic compounds. 1,2-dichloro-4-(trifluoroMethoxy)benzene is considered to be toxic if ingested, inhaled, or absorbed through the skin, and should be handled with care. Additionally, it is classified as a hazardous substance and should be stored and disposed of properly according to regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 151276-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,2,7 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 151276-10:
(8*1)+(7*5)+(6*1)+(5*2)+(4*7)+(3*6)+(2*1)+(1*0)=107
107 % 10 = 7
So 151276-10-7 is a valid CAS Registry Number.

151276-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Dichloro-4-(trifluoromethoxy)benzene

1.2 Other means of identification

Product number -
Other names 3,4-dichloro-trifluoromethoxybenzene

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:151276-10-7 SDS

151276-10-7Downstream Products

151276-10-7Relevant articles and documents

Silver-Mediated Trifluoromethoxylation of (Hetero)aryldiazonium Tetrafluoroborates

Yang, Yu-Ming,Yao, Jian-Fei,Yan, Wei,Luo, Zhuangzhu,Tang, Zhen-Yu

supporting information, p. 8003 - 8007 (2019/10/11)

Here we report a silver-mediated trifluoromethoxylation of (hetero)aryldiazonium tetrafluoroborates by converting an aromatic amino group into an OCF3 group. This method, which can be considered to be a trifluoromethoxylation variation of the classic Sandmeyer-type reaction, uses readily available aryl and heteroaromatic amines as starting materials and AgOCF3 as trifluoromethoxylating reagents. The broad substrate scope and simple, mild reaction condition made this transformation a valuable method in constructing aryl-OCF3 bonds.

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