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2-ethyl-4-hydroxyphenyl thiocyanate is a chemical compound with the molecular formula C10H11NOS. It is known for its ability to impart a particular odor to products and is commonly used as an intermediate in the synthesis of various organic compounds.

6291-20-9

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6291-20-9 Usage

Uses

Used in Perfume and Personal Care Industry:
2-ethyl-4-hydroxyphenyl thiocyanate is used as a fragrance ingredient for its appealing scent, enhancing the overall aroma of perfumes and personal care products.
Used in Hair Care Industry:
In hair care products, 2-ethyl-4-hydroxyphenyl thiocyanate is used to mask unpleasant odors, providing a fresh and pleasant scent to hair care formulations.
Used in Cleaning Products Industry:
2-ethyl-4-hydroxyphenyl thiocyanate is utilized in the manufacturing of cleaning products due to its fragrance and antibacterial properties, making it an effective component for creating clean and fresh-smelling environments.

Check Digit Verification of cas no

The CAS Registry Mumber 6291-20-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6291-20:
(6*6)+(5*2)+(4*9)+(3*1)+(2*2)+(1*0)=89
89 % 10 = 9
So 6291-20-9 is a valid CAS Registry Number.

6291-20-9SDS

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 (2-ethyl-4-hydroxyphenyl) thiocyanate

1.2 Other means of identification

Product number -
Other names 2-ethyl-4-hydroxyphenyl thiocyanate

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:6291-20-9 SDS

6291-20-9Downstream Products

6291-20-9Relevant academic research and scientific papers

N-doped ZnO as an efficient photocatalyst for thiocyanation of indoles and phenols under visible-light

Hosseini-Sarvari, Mona,Sarvestani, Abdollah Masoudi

, p. 903 - 911 (2021/07/17)

In this study, nitrogen-doped ZnO nanorods (N–ZnO NRs) were synthesized via a very simple hydrothermal process, fully characterized, and this photocatalyst was successfully exploited in thiocyanation reactions of indoles and phenols at room temperature under visible light irradiation. Two important classes of aromatic compounds indoles, and phenols using N–ZnO NRs as photocatalyst treated with ammonium thiocyanate as thiocyanation agent formed the corresponding thiocyano compounds in good yields. Nitrogen is one of the most appropriate p-type dopants that is nontoxic, similar to the atomic radius to oxygen, and lower electronegativity and ionization energy than the O atom. Therefore, the N doping converts ZnO into the p-type ZnO semiconductor structure. This potent, simple, and versatile protocol afforded thiocyanation reactions of indole and phenols under visible light. The reactions proceeded through a radical pathway by applying air molecular oxygen as a low cost and environmentally friendly terminal oxidant. The proposed mechanism based on control experiments was thoroughly described. Graphic abstract: [Figure not available: see fulltext.]

ARS-TiO2 photocatalyzed direct functionalization of sp2 C-H bonds toward thiocyanation and cyclization reactions under visible light

Hosseini-Sarvari, Mona,Hosseinpour, Zeinab,Koohgard, Mehdi,Sarvestani, Abdollah Masoudi

, p. 1401 - 1407 (2020/03/26)

An ARS-TiO2 photocatalyst has been prepared, by a simple method through stirring a mixture of ARS and TiO2 at room temperature in the dark, to extend the photocatalytic response of titanium dioxide toward the visible light spectrum. The synergic effect of ARS and TiO2 in the photocatalyst system has catalyzed direct C-H functionalization of sp2 C-H bonds toward thiocyanation and cyclization reactions. Several aromatic and heteroaromatic scaffolds (2-phenylamino-thiazole, phenol, aniline, indole and pyrrole derivatives) were treated with the thiocyanate anion at room temperature. Herein, the first report on thiocyanation of phenol and synthesis of 2-aminobenzothiazole derivatives under visible light is presented.

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