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1-(2-fluorobenzyl)-3-(3-methoxyphenyl)-1-(tetrahydrofuran-2-ylmethyl)thiourea is a complex organic compound with the molecular formula C20H22FN2O2S. It features a thiourea core, which is a sulfur-containing analog of urea, and is characterized by the presence of a 2-fluorobenzyl group, a 3-methoxyphenyl group, and a tetrahydrofuran-2-ylmethyl group. This chemical is a member of the thiourea class and is known for its potential applications in pharmaceuticals and agrochemicals due to its unique structure and properties. The compound's specific arrangement of functional groups and its fluorinated and oxygenated components contribute to its reactivity and potential therapeutic or pesticidal activity.

6175-48-0

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6175-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6175-48-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,7 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6175-48:
(6*6)+(5*1)+(4*7)+(3*5)+(2*4)+(1*8)=100
100 % 10 = 0
So 6175-48-0 is a valid CAS Registry Number.

6175-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2-fluorophenyl)methyl]-3-(3-methoxyphenyl)-1-(oxolan-2-ylmethyl)thiourea

1.2 Other means of identification

Product number -
Other names 3-Aethyl-octan-2-on

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:6175-48-0 SDS

6175-48-0Downstream Products

6175-48-0Relevant articles and documents

Highly productive α-alkylation of ketones with alcohols mediated by an Ir-oxalamidato/solid base catalyst system

Maeda, Hironori,Nara, Hideki,Shimizu, Hideo

supporting information, p. 2772 - 2779 (2020/12/29)

An Ir-oxalamidato complex in combination with a solid base (e.g., magnesium aluminometasilicate/Ca(OH)2) significantly improved the catalyst productivity in α-alkylation of methyl ketones with primary alcohols. Optimization through systematic variation of the oxalamidato ligand led to a practical turnover number (TON) of 10 000.40 000.

Preparation of Organozinc and Organocadmium Compounds from the Metals and Alkyl Halides in the Presence of Stimulating Systems Based on a Derivative a Transition Metal and an Organometallic Compound

Eremeev,Danov,Skudin,Sakhipov

, p. 556 - 559 (2007/10/03)

Full and mixed alkyl derivatives of zinc and cadmium were prepared from these metals and organic halides in the presence of stimulating systems necessarily containing a transition metal derivative and an organometallic compound capable of reducing this derivative under the process conditions. Such stimulating systems make it possible to introduce selectively organic halides (iodides, bromides, chlorides) into the reaction with zinc and cadmium to obtain the corresponding mixed organometallic compounds.

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