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3-Furanethanol, 2-(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89861-16-5

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89861-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89861-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,6 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89861-16:
(7*8)+(6*9)+(5*8)+(4*6)+(3*1)+(2*1)+(1*6)=185
185 % 10 = 5
So 89861-16-5 is a valid CAS Registry Number.

89861-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-phenylsulfanylfuran-3-yl)ethanol

1.2 Other means of identification

Product number -
Other names -

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:89861-16-5 SDS

89861-16-5Relevant academic research and scientific papers

Rapid construction of the aza-propellane core of acutumine via a photochemical [2 + 2] cycloaddition reaction

Navarro, Raul,Reisman, Sarah E.

supporting information, p. 4354 - 4357 (2012/11/07)

Synthetic efforts toward the chlorinated aza-propellane alkaloid acutumine (1) are described. The key vicinal quaternary centers were constructed by a photochemical [2 + 2] cycloaddition reaction of a furanyl-tetrahydroindolone. Dihydroxylation of the [2

3-ALKYLFURANS AS USEFUL SYNTHETIC EQUIVALENTS FOR SUBSTITUTED Δ2-BUTENOLIDES

Goldsmith, David,Liotta, Dennis,Saindane, Manohar,Waykole, Liladhar,Bowen, Phillip

, p. 5835 - 5838 (2007/10/02)

Substituted Δ2-butenolides may be prepared from furan equivalents by regiospecific metallation, sulfenylation and/or silylation, removal of the sulfur group and peracid oxidation.

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