Welcome to LookChem.com Sign In|Join Free
  • or
Hexahydro-1,3-benzodithiole-2-thione is a chemical compound with the molecular formula C6H8NS2. It is a heterocyclic compound, which means it contains atoms of different elements in its ring structure. Specifically, hexahydro-1,3-benzodithiole-2-thione features a benzene ring fused to a dithiole ring, with the latter containing two sulfur atoms. The compound has a thioketone functional group, indicated by the -thione suffix, which means it has a carbon-sulfur double bond. This chemical is known for its potential applications in the synthesis of various organic compounds and as an intermediate in pharmaceutical and agrochemical industries. It is also recognized for its unique chemical properties, such as its reactivity and stability, which make it a subject of interest in organic chemistry research.

2164-87-6

Post Buying Request

2164-87-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2164-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2164-87-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2164-87:
(6*2)+(5*1)+(4*6)+(3*4)+(2*8)+(1*7)=76
76 % 10 = 6
So 2164-87-6 is a valid CAS Registry Number.

2164-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3a,4,5,6,7,7a-hexahydrobenzo[d][1,3]dithiole-2-thione

1.2 Other means of identification

Product number -
Other names trans-3a,4,5,6,7,7a-Hexahydro-2H-1,3-benzodithiole-2-thione

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:2164-87-6 SDS

2164-87-6Relevant academic research and scientific papers

Convenient procedure for converting 1,3-dithiolane-2-thiones into 1,3-dithiolan-2-ones

Barbero, Margherita,Degani, Iacopo,Dughera, Stefano,Fochi, Rita,Piscopo, Laura

, p. 289 - 294 (2007/10/03)

1,3-Dithiolan-2-ones have been obtained by reaction of 1,3-dithiolane-2-thiones and epoxides in the presence of HBF4·Et2O. The reactions, carried out in anhydrous CH2Cl2 at 0-5°C→room temperature (Procedure A) or in anhydrous chlorobenzene at 0-5→80°C (Procedure B), gave product yields of 63-95%. By Procedure B it was also possible to isolate the intermediates 1-oxa-4,6,9-trithiaspiro[4,4]nonanes in good yields (66-85%). Reaction pathways are proposed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2164-87-6