16486-30-9

Usage

Uses

Used in Chemical Synthesis:
(1-methylethyl)carbamodithioic acid propan-2-amine (1:1) is utilized as a reagent in the synthesis of other chemicals and pharmaceuticals. Its chelating ability and interaction with proteins and enzymes make it a valuable component in creating new compounds with specific properties.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (1-methylethyl)carbamodithioic acid propan-2-amine (1:1) is used as a precursor for the development of new drugs. Its capacity to bind with metal ions and interact with biological molecules can lead to the creation of medications with targeted effects.
Used in Industrial Applications:
(1-methylethyl)carbamodithioic acid propan-2-amine (1:1) is employed as a chelating agent in various industrial processes. Its ability to form complexes with metal ions can improve the efficiency of certain manufacturing procedures.
Used in Agriculture:
In agricultural settings, (1-methylethyl)carbamodithioic acid propan-2-amine (1:1) is used for its antimicrobial and antifungal properties. It can help protect crops from diseases and pests, contributing to increased yields and crop health.
Used in Antimicrobial Agents:
(1-methylethyl)carbamodithioic acid propan-2-amine (1:1) is used as an antimicrobial agent in different applications, such as in the production of sanitizing products or as a preservative in various goods. Its ability to combat microorganisms makes it a useful component in these products.
Safety Precautions:
It is crucial to handle (1-methylethyl)carbamodithioic acid propan-2-amine (1:1) with care, as it can be hazardous if not used properly. Adequate safety measures should be taken to minimize risks during its use in various applications.

Upstream product

• 75-15-0 carbon disulfide 
• 3332-08-9 2-isopropyliminopropane 
• 75-31-0 isopropylamine 

Downstream Products

• 2986-17-6 1,3-diisopropylthiourea 
• 95754-26-0 3-isopropyl-5-phenyl-2-thioxo-1,3-thiazolidine-4-one 
• 277301-82-3 N-tert-butyl-2-phenyl-2-<(N-isopropylthiocarbamoyl)thio>acetamide 
• 277301-81-2 N-(4-methylphenyl)-2-phenyl-2-<(N-isopropylthiocarbamoyl)thio>acetamide 
• 277301-83-4 N-(4-methylphenyl)-2-<(N-isopropylthiocarbamoyl)thio>propionamide 
• 17294-24-5 3-isopropyl-4-phenyl-5-methyl-Δ⁴-1,3-thiazoline-2-thione 

Relevant academic research and scientific papers

4-Aryl-2-Imino-1,3-Dithiolanes from the Room Temperature Coupling of Sodium Dithiocarbamates with Sulfonium Salts

A series of 4-aryl-2-imino-1,3-dithiolanes was synthesized by means of a straightforward strategy starting from readily available precursors: reactions of dithiocarbamates and arylsulfonium salts, at room temperature in water/CH2Cl2 as biphasic medium, afforded the five-membered cyclic products in good yields. The reaction mechanism was investigated by DFT calculations.

Cu-mediated one-pot three-component synthesis of 3-N-substituted 1,4,2-benzodithiazine 1,1-dioxide derivatives

A novel and efficient copper-catalyzed one-pot procedure for the synthesis of 3-N-substituted 1,4,2-benzodithiazine 1,1-dioxide derivatives from 2-halobenzenesulfonamides, amines and CS2 is described. The reaction proceeds through Ullmann-type S-arylation, intramolecular addition of NH2 with C[dbnd]S and dehydrosulfide, which provides a new and useful strategy for construction of cyclic aromatic sulfonamides.

The Crystal and Molecular Structure of 3-Isopropyl-5-phenylrhodanide

3-Isopropyl-5-phenylthiazolidin-4-one-2-thione crystallizes in the monoclinic space group P21.The structure has been determined by single crystal X-ray diffraction and refined to R=0.022 and Rw=0.025.The bond lengths of the CO-N-CS-S part are discussed in relation to MO calculations.The 3-isopropyl group is bisected by the thiazolidine ring plane , with the methyl groups turned towards the carbonyl oxygen, as expected from steric considerations.The thiazolidine and phenyl rings are practically planar with an 86.2 grad angle between the planes.