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Thiocyanic acid, 2-hydroxy-2,2-diphenylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61807-33-8

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61807-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61807-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,0 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61807-33:
(7*6)+(6*1)+(5*8)+(4*0)+(3*7)+(2*3)+(1*3)=118
118 % 10 = 8
So 61807-33-8 is a valid CAS Registry Number.

61807-33-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-diphenyl-2-thiocyano ethanol

1.2 Other means of identification

Product number -
Other names 1-Hydroxy-1,1-diphenyl-2-thiocyanato-ethan

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:61807-33-8 SDS

61807-33-8Downstream Products

61807-33-8Relevant academic research and scientific papers

Photocatalytic anion oxidation achieves direct aerobic difunctionalization of alkenes leading to β-thiocyanato alcohols

Zhang, Wei,Guo, Jun-Tao,Yu, Yue,Guan, Zhi,He, Yan-Hong

, p. 3038 - 3044 (2018/05/16)

A novel visible light-driven oxidative cascade reaction for the synthesis of β-thiocyanato alcohols via difunctionalization of alkenes is described for the first time. In this protocol inorganic ion thiocyanate was successfully converted into radical through photocatalysis by employing Rose Bengal as a photocatalyst to mediate the single-electron transfer. This hydroxylation process did not need extra reducing agent and the new C–S and C–O bonds could be constructed in one pot. Molecular oxygen not only was used as an excellent terminal oxidant, but also served as a green oxygen source, which is one of the most ideal processes to realize C–H bond oxidation functionalization. Moreover, the reaction also proceeded very well under irradiation of sunlight.

1,1-Diphenyl-2-methylsulfinyl ethanol: A model compound to study the reactivity towards CNBr of a photoadduct of methionine on CγH2

Sachon, Emmanuelle,Milcent, Thierry,Sagan, Sandrine,Convert, Odile,Chassaing, Gérard,Lavielle, Solange

, p. 7485 - 7489 (2007/10/03)

The photoadduct formed by photolysis of the [Bapa0, (pBzl)Phe5, Met(O2)11]SP/NK-1 complex localised within the T173MP175 domain of the NK-1 receptor cannot be cleaved by CNBr on the C-side of methionine; an unusual rearrangement of the intermediate sulfonium instead occurred. The reactivity of 1,1-diphenyl-2-methylsulfinyl ethanol 10 towards CNBr treatment and the stability of the 1,1-diphenyl oxirane 14 were analysed by NMR and mass spectrometry. 1,1-Diphenyl ethylene 13 can be formed from epoxide 14 even in slightly acidic conditions and during positive DCI/NH3 mass spectrometry analysis. Altogether, these results suggest that if a covalent linkage between the [Bapa0, (pBzl)Phe5, Met(O2)11] and the NK-1 receptor occurred on the CγH2 of methionine-174, CNBr treatment will lead to an epoxide/ketone and an ethylenic compound.

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