16486-30-9

Basic information

• Product Name: (1-methylethyl)carbamodithioic acid - propan-2-amine (1:1)
• CAS NO: 16486-30-9
• Molecular Formula: C₃H₉N*C₄H₉NS₂
• Molecular Weight: 194.3612
• Mol File: 16486-30-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 159.7°C at 760 mmHg
• Flash Point: 50.4°C
• Vapor Pressure: 2.47mmHg at 25°C
• CAS DataBase Reference: (1-methylethyl)carbamodithioic acid - propan-2-amine (1:1)(CAS DataBase Reference)
• NIST Chemistry Reference: (1-methylethyl)carbamodithioic acid - propan-2-amine (1:1)(16486-30-9)
• EPA Substance Registry System: (1-methylethyl)carbamodithioic acid - propan-2-amine (1:1)(16486-30-9)

Safety Data

• Hazardous Substances Data: 16486-30-9(Hazardous Substances Data)

Usage

General Description

(1-methylethyl)carbamodithioic acid - propan-2-amine (1:1) is a chemical compound that consists of equal parts of (1-methylethyl)carbamodithioic acid and propan-2-amine. (1-methylethyl)carbamodithioic acid - propan-2-amine (1:1) is commonly used in the synthesis of other chemicals and pharmaceuticals. It acts as a chelating agent, meaning it can bind to metal ions to form complexes, and it also has potential biological applications due to its ability to interact with proteins and enzymes. Additionally, it has been found to have antimicrobial and antifungal properties, making it useful in various industrial and agricultural applications. However, it is important to handle this compound with care, as it can be hazardous if not used properly.

Upstream product

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

Downstream Products

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

Relevant articles and documents

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.

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.