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8-Thiabicyclo[5.1.0]octane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53907-79-2

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53907-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53907-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,0 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53907-79:
(7*5)+(6*3)+(5*9)+(4*0)+(3*7)+(2*7)+(1*9)=142
142 % 10 = 2
So 53907-79-2 is a valid CAS Registry Number.

53907-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-thiabicyclo[5.1.0]octane

1.2 Other means of identification

Product number -
Other names 8-thia-bicyclo[5.1.0]octane

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:53907-79-2 SDS

53907-79-2Downstream Products

53907-79-2Relevant academic research and scientific papers

An efficient and improved method for the conversion of oxiranes into thiiranes using graphite oxide

Mirza-Aghayan, Maryam,Molaee Tavana, Mahdieh

, p. 30 - 35 (2015/10/20)

An efficient and improved procedure has been developed for the conversion of oxiranes into thiiranes using sodium thiocyanate in the presence of graphite oxide under solvent-free conditions at an ambient temperature in excellent yields and in short reaction times.

Odourless strategy for deep eutectic solvent-mediated ring opening of epoxides with in situ generated S -alkylisothiouronium salts

Azizi, Najmedin,Yadollahy, Zahra,Rahimzadeh-Oskooee, Amin

, p. 1085 - 1088 (2014/05/20)

A general, straightforward and odourless ring-opening reaction allows the preparation of β-hydroxy sulfides from in situ generated S-alkylisothiouronium salts in urea-choline chloride-based deep eutectic solvent (DES). In addition, reaction of epoxides with thiourea in DES yields the corresponding thiiranes. Georg Thieme Verlag Stuttgart New York.

Direct episulfidation of alkenes and allenes with elemental sulfur and thiiranes as sulfur sources, catalyzed by molybdenum oxo complexes

Adam, Waldemar,Bargon, Rainer M.,Schenk, Wolfdieter A.

, p. 3871 - 3876 (2007/10/03)

The molybdenum oxo complexes 1a and 1b catalyze efficiently the sulfur transfer to a series of alkenes 4 and allenes 6, for which elemental sulfur, phenylthiirane, or methylthiirane have been employed as sulfur sources to afford the corresponding episulfi

Synthesis of thiiranes through direct sulfur transfer to cycloalkenes in the thermolysis of a thiophene endoperoxide

Adam, Waldemar,Weinkoetz, Stephan

, p. 177 - 178 (2007/10/03)

Thiophene endoperoxide 2, which was prepared by photo-oxygenation of thiophene 1, transfers a sulfur atom to form thiiranes when thermolysed in the presence of cycloalkenes, an unexpectedly efficient process which can be catalysed by the cobalt-tetraphenylporphine complex.

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