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5-(BENZO-[B]-THIOPHEN-3-YL)-3-(TRIFLUOROMETHYL)PYRAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

4099-11-0

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4099-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4099-11-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,9 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4099-11:
(6*4)+(5*0)+(4*9)+(3*9)+(2*1)+(1*1)=90
90 % 10 = 0
So 4099-11-0 is a valid CAS Registry Number.

4099-11-0SDS

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 3-(1-benzothiophen-3-yl)-5-(trifluoromethyl)-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 5-(benzo-[b]-thiophen-3-yl)-3-(trifluoromethyl)pyrazole

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:4099-11-0 SDS

4099-11-0Downstream Products

4099-11-0Relevant academic research and scientific papers

Regioselective Synthesis of 3-Trifluoromethylpyrazole by Coupling of Aldehydes, Sulfonyl Hydrazides, and 2-Bromo-3,3,3-trifluoropropene

Zhu, Chuanle,Zeng, Hao,Liu, Chi,Cai, Yingying,Fang, Xiaojie,Jiang, Huanfeng

supporting information, p. 809 - 813 (2020/02/04)

A general and practical strategy for 3-trifluoromethylpyrazole synthesis is reported that occurs by the three-component coupling of environmentally friendly and large-tonnage industrial feedstock 2-bromo-3,3,3-trifluoropropene (BTP), aldehydes, and sulfonyl hydrazides. This highly regioselective three-component reaction is metal-free, catalyst-free, and operationally simple and features mild conditions, a broad substrate scope, high yields, and valuable functional group tolerance. Remarkably, the reactions could be performed on a 100 mmol scale and smoothly afforded the key intermediates for the synthesis of celecoxib, mavacoxib, SC-560, and AS-136A. Preliminary mechanism studies indicated that a 1,3-hydrogen atom transfer process was involved in this transformation.

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