Welcome to LookChem.com Sign In|Join Free
  • or
2-ISOBUTYL-1,3-DITHIANE is a dithiophosphine compound with the molecular formula C6H12S2. It features a six-membered ring with two sulfur atoms and an isobutyl group attached at the 2-position. This chemical compound is recognized for its unique reactivity and high functional group tolerance, making it a versatile and important reagent in organic synthesis.

69824-23-3

Post Buying Request

69824-23-3 Suppliers

Recommended suppliers

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

69824-23-3 Usage

Uses

Used in Pharmaceutical Industry:
2-ISOBUTYL-1,3-DITHIANE is used as a synthetic intermediate for the preparation of various pharmaceuticals. It serves as a building block in the synthesis of biologically active compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 2-ISOBUTYL-1,3-DITHIANE is utilized as a key intermediate in the synthesis of agrochemicals. Its role in creating compounds with pesticidal or herbicidal properties aids in enhancing crop protection and yield.
Used in Organic Synthesis:
2-ISOBUTYL-1,3-DITHIANE is employed as a versatile reagent in organic synthesis, where its unique reactivity and functional group tolerance are leveraged to facilitate the creation of a wide range of chemical compounds for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 69824-23-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,2 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69824-23:
(7*6)+(6*9)+(5*8)+(4*2)+(3*4)+(2*2)+(1*3)=163
163 % 10 = 3
So 69824-23-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H16S2/c1-7(2)6-8-9-4-3-5-10-8/h7-8H,3-6H2,1-2H3

69824-23-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B21471)  2-Isobutyl-1,3-dithiane, 97%   

  • 69824-23-3

  • 5g

  • 186.0CNY

  • Detail
  • Alfa Aesar

  • (B21471)  2-Isobutyl-1,3-dithiane, 97%   

  • 69824-23-3

  • 25g

  • 719.0CNY

  • Detail
  • Alfa Aesar

  • (B21471)  2-Isobutyl-1,3-dithiane, 97%   

  • 69824-23-3

  • 100g

  • 2418.0CNY

  • Detail

69824-23-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylpropyl)-1,3-dithiane

1.2 Other means of identification

Product number -
Other names 2-ISOBUTYL-1,3-DITHIANE

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:69824-23-3 SDS

69824-23-3Relevant academic research and scientific papers

Identification and synthesis of homoterpenoids emitted from elm leaves after elicitation by beetle eggs

Wegener, Robert,Schulz, Stefan

, p. 315 - 319 (2002)

Egg deposition of the elm leaf beetle Xanthogaleruca luteola on the leaves of the field elm causes the emission of volatiles attracting the parasitoid Oomyzus gallerucae. The present study describes the identification and synthesis of the homoterpenoids:

Boric acid compound, borate compound and their preparation methods and application

-

Paragraph 0172; 0173, (2018/12/02)

The invention provides a boric acid compound and a borate compound shown as formula I and formula II which are shown in the description, and their preparation methods, application and pharmaceutical compositions. The boric acid compound and the borate compound can inhibit proteasome and are suitable for treating multiple myeloma.

Synthesis of (-)-idiadione, a furanosesterterpene isolated from a marine sponge Spongia idia

Noda, Yoshihiro,Hashimoto, Hiroyuki,Norizuki, Toshie

, p. 1839 - 1841 (2007/10/03)

(-)-Idiadione (1) , a furanosesterterpene isolated from a marine sponge Spongia idia, was synthesized, starting from (S)-(-)-citronellal (2). The absolute configuration of naturally occurring 1 is established as (S).

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 69824-23-3