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1,3-Dithiane, 2-ethyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39854-50-7

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39854-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39854-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,5 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39854-50:
(7*3)+(6*9)+(5*8)+(4*5)+(3*4)+(2*5)+(1*0)=157
157 % 10 = 7
So 39854-50-7 is a valid CAS Registry Number.

39854-50-7SDS

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 2-ethyl-2-phenyl-1,3-dithiane

1.2 Other means of identification

Product number -
Other names 2-Ethyl-2-phenyl-1,3-dithian

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:39854-50-7 SDS

39854-50-7Relevant academic research and scientific papers

Thioacetalization of aldehydes and ketones catalyzed by hexabromoacetone

Chaiseeda, Kittichai,Chavasiri, Warinthorn

, p. 1034 - 1039 (2017)

Protection of p-anisaldehydewith 1,3-propanedithiol under UV irradiation without a catalyst resulted in 87% yield of 1,3-dithiane in 20 min. Addition of hexabromoacetone further reduced the reaction time and UV irradiation also accelerated the formation o

An efficient, continuous flow technique for the chemoselective synthesis of thioacetals

Wiles, Charlotte,Watts, Paul,Haswell, Stephen J.

, p. 7362 - 7365 (2008/03/13)

By optimizing a reagent's residence time within a packed-bed reactor, it is possible to overcome selectivity issues frequently encountered in stirred reaction vessels. This important feature is demonstrated for the chemoselective protection of 4-acetylben

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