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69824-23-3

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69824-23-3 Usage

General Description

2-ISOBUTYL-1,3-DITHIANE is a chemical compound with the molecular formula C6H12S2. It is a dithiophosphine compound, consisting of a six-membered ring with two sulfur atoms and an isobutyl group attached at the 2-position. 2-ISOBUTYL-1,3-DITHIANE is used primarily as a synthetic intermediate in organic chemistry, particularly in the preparation of pharmaceuticals and agrochemicals. Its main applications include its use as a building block in the synthesis of various biologically active compounds. 2-ISOBUTYL-1,3-DITHIANE is considered to be a versatile and important chemical reagent in organic synthesis due to its unique reactivity and high functional group tolerance.

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

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  • 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 articles and documents

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:

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).

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