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370-47-8

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370-47-8 Usage

Appearance

Yellow solid
A visually distinguishable, solid-state form with a yellow color.

Usage in synthesis

Pharmaceutical and organic compounds
This compound serves as a building block or intermediate in the production of pharmaceuticals and other organic compounds.

Structural components

Nitro group, trifluoromethyl group, thioether group, and benzene ring
The compound's structure consists of these functional groups attached to a benzene ring.

Usage in production

Agrochemicals, dyes, and specialty chemicals
Due to its unique chemical properties, 1-nitro-3-[(trifluoromethyl)thio]benzene is used in the manufacturing of agrochemicals, dyes, and other specialty chemicals.

Potential applications

Synthesis of materials and as a reagent in organic chemical reactions
The compound may have further applications in the synthesis of materials and as a reagent to facilitate organic chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 370-47-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 370-47:
(5*3)+(4*7)+(3*0)+(2*4)+(1*7)=58
58 % 10 = 8
So 370-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H4F3NO2S/c8-7(9,10)14-6-3-1-2-5(4-6)11(12)13/h1-4H

370-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-nitro-3-(trifluoromethylsulfanyl)benzene

1.2 Other means of identification

Product number -
Other names (3-Nitro-phenyl)-trifluormethyl-sulfid

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:370-47-8 SDS

370-47-8Relevant articles and documents

BORON CONTAINING COMPOUNDS AND THEIR USES

-

, (2022/03/07)

The present disclosure relates to novel boron-containing compounds and their novel uses, e.g., as active ingredients that have pesticidal activity. The disclosure also relates to agrochemical compositions and their use in agriculture or horticulture for the control or prevention of infestation of plants, plant parts, plant propagation materials, harvested food crops, or seeds by pests, specifically fungi and nematodes. The disclosure further relates to methods for promoting plant performance and/or curatively or preventively controlling phytopathogens, (particularly fungi and nematodes) on or in a plant, plant parts, plant propagation materials, seeds, harvested fruits, or vegetables.

Copper(I)-promoted trifluoromethylthiolation of arenediazonium salts with AgSCF3

Zheng, Changge,Liu, Yang,Hong, Jianquan,Huang, Shuai,Zhang, Wei,Yang, Yupeng,Fang, Ge

, p. 1404 - 1407 (2019/05/01)

An efficient method for trifluoromethylthiolation of arenediazonium salts has been developed in mild conditions with a stable and convenient AgSCF3. It provides a straightforward and convenient way for the synthesis of trifluoromethylthiolated compound from diazonium salts in moderate to good yields.

Cu-mediated oxidative trifluoromethylthiolation of arylboronic acids with (bpy)CuSCF3

Zhao, Mingzhu,Zhao, Xiaoming,Zheng, Purui,Tian, Yawei

, p. 73 - 79 (2017/01/17)

An efficient trifluoromethylthiolation reaction of arylboronic acids with (bpy)CuSCF3in the presence of oxygen at room temperature is described. This method produces a variety of aryl trifluoromethylthioether derivatives in good to high yield. The mechanism of this trifluoromethylthiolation is discussed as well.

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