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Bicyclo[2.2.1]heptane-2,3-dithiol, (exo,exo)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23657-28-5

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23657-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23657-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,5 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23657-28:
(7*2)+(6*3)+(5*6)+(4*5)+(3*7)+(2*2)+(1*8)=115
115 % 10 = 5
So 23657-28-5 is a valid CAS Registry Number.

23657-28-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo{2.2.1}hepta-exo-cis-2,3-dithiol

1.2 Other means of identification

Product number -
Other names norbornane-exo-2,3-dithiol

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:23657-28-5 SDS

23657-28-5Downstream Products

23657-28-5Relevant academic research and scientific papers

Conversion of norbornene derivatives into vicinal-dithioethers via S 8 activation

Poulain, Sophie,Julien, Sandy,Du?ach, Elisabet

, p. 7077 - 7079 (2005)

Norbornene reacts with elemental sulfur to give a mixture of trithiolane and pentathiepane. Sulfuration of norbornene derivatives was achieved with elemental sulfur, by using a catalytic amount of a nickel complex, to afford selectively the corresponding trithiolanes. The most effective catalytic system was Ni(NH3)6Cl2 in dimethylformamide. The trithiolanes were reduced with super-hydride into 1,2-dithiolate salts, and quenched in situ to form vicinal-dithioethers.

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