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83521-64-6

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83521-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83521-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,2 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83521-64:
(7*8)+(6*3)+(5*5)+(4*2)+(3*1)+(2*6)+(1*4)=126
126 % 10 = 6
So 83521-64-6 is a valid CAS Registry Number.

83521-64-6SDS

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 2-(p-fluorophenyl)-1,3-Dithiolane

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:83521-64-6 SDS

83521-64-6Downstream Products

83521-64-6Relevant articles and documents

Aluminum hydrogen sulfate [Al(HSO4)3] as an efficient catalyst for the preparation of thioacetals

Ghashang, Majid

, p. 2837 - 2842 (2013/07/26)

Aluminum hydrogen sulfate, as a heterogeneous solid acid catalyst, has been used for the mild conversion of carbonyl compounds to their thioacetals using 1,2- and 1,3-dithiol under ambient conditions with short reaction times in high to excellent yield in

Chemoselective dithioacetalization of carbonyl compounds using magnesium hydrogensulfate as efficient heterogeneous catalyst

Shaterian, Hamid Reza,Hosseinian, Asghar,Ghashang, Majid,Khorami, Fahimeh

experimental part, p. 2490 - 2501 (2009/08/07)

Carbonyl compounds have been successfully converted into their corresponding dithiolanes and dithianes derivatives with 1,2-ethanedithiol and 1,3-propanedithiol in excellent yield at room temperature and short reaction times using a catalytic amount of ma

Trichloromelamine (TCM) - Catalyzed efficient and selective thioacetalization of aldehydes and transthioacetalization of acetals and oxathioacetals under mild reaction conditions

Hazarkhani, Hassan

, p. 2597 - 2606 (2008/12/22)

Trichloromelamine was used effectively as a catalyst for thioacetalization of aldehydes and transthioacetalization of acetals and oxathioacetals under mild and almost neutral reaction conditions. By this method, aldehydes, acetals, and oxathioacetals were selectively protected in the presence of ketones as their 1,3-dithiolanes or 1,3-dithianes. Copyright Taylor & Francis Group, LLC.

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