20607-43-6

Basic information

• Product Name: SODIUM 2-PROPANETHIOLATE
• Synonyms: SODIUM 2-PROPANETHIOLATE;2-PROPANETHIOL SODIUM SALT;SodiuM 2-propanethiolate technical, >=90.0% (RT);2-Propanethiol, sodium salt (8CI,9CI)
• CAS NO: 20607-43-6
• Molecular Formula: C₃H₇S*Na
• Molecular Weight: 98.14
• Mol File: 20607-43-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• BRN: 3618618
• CAS DataBase Reference: SODIUM 2-PROPANETHIOLATE(CAS DataBase Reference)
• NIST Chemistry Reference: SODIUM 2-PROPANETHIOLATE(20607-43-6)
• EPA Substance Registry System: SODIUM 2-PROPANETHIOLATE(20607-43-6)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45
• RIDADR: UN 3263 8/PG 3
• WGK Germany: 3
• F: 1-10-13
• HazardClass: 4.3
• PackingGroup: III
• Hazardous Substances Data: 20607-43-6(Hazardous Substances Data)

Usage

General Description

Sodium 2-propanethiolate is a chemical compound with the molecular formula C3H7NaS. It is the sodium salt of 2-propanethiol, a thiol compound with a strong, unpleasant odor. Sodium 2-propanethiolate is used in organic synthesis as a reagent for the preparation of various organic compounds, including thioethers, sulfides, and thioesters. It is also used in the manufacturing of pharmaceuticals, pesticides, and other industrial products. The compound is typically a white to off-white solid and is soluble in water, making it easy to handle and use in laboratory and industrial settings. However, it is important to handle sodium 2-propanethiolate with care, as it can be toxic if ingested or inhaled and can cause irritation to the skin and eyes.

InChI:InChI=1/C3H8S.Na/c1-3(2)4;/h3-4H,1-2H3;/q;+1/p-1/rC3H7NaS/c1-3(2)5-4/h3H,1-2H3

Upstream product

• 75-33-2 2-propanethiol 

Downstream Products

• 14272-25-4 isopropyl propargyl sulfide 
• 99064-14-9 cyclohex-2-enyl-isopropyl sulfide 
• 40811-49-2 2-(1-methylethylthio)ethanol 
• 18267-22-6 i-propyl 4-methylbenzylsulfide 
• 18888-46-5 isopropyl vinyl sulfide 
• 98626-93-8 5-bromo-2-isopropylsulfanyl-pyridine 
• 98627-05-5 2,3-bis(isopropylthio)pyridine 
• 25752-81-2 C₁₅H₁₈N₂O₄S₃ 
• 103653-41-4 C₁₅H₁₆Br₂N₂O₄S₃ 
• 74542-69-1 1,2,4,5-Tetrakis(isopropylthio)benzene 
• 70416-07-8 1,2,4,6-tetrakis(isopropylthio)benzene 
• 74542-67-9 1,3,5-Trisbenzene 
• 7205-62-1 1-chloro-4-(isopropylthio)benzene 
• 70398-85-5 1,4-Bisbenzene 

Relevant articles and documents

Design and synthesis of new 4-alkylthio monocyclic β-lactams

New types of monocyclic β-lactams constitute an important class of compounds due to their unique structures and natures. Here, the design and synthesis of new 4-alkylthio monocyclic β-lactams 2a and 3a are reported. Significantly, compounds 2a and 3a, while keeping a monocyclic system, were designed to contain all of the substructures provided by the cleavage of C(2)-C(3) bond in penicillins. Efficient synthetic pathways for compounds 2a and 3a were established based on two different strategies. Compound 2a was synthesized from raw materials, using 4-acetoxyazetidin-2-one as a key intermediate, through a ten-step synthetic sequence in 3% overall yield. Compound 3a was synthesized from potassium salt of penicillin G (17), using the degraded product 20 as a key intermediate, through a six-step synthetic sequence in 11% overall yield. 4-Alkylthioazetidin- 2-one derivatives, introduced in this study, could serve as valuable intermediates for the development of new monocyclic β-lactams.

Process for producing arylsulfenyl halide

A process for producing a compound of the formula (II): wherein Hal1 represents halogen and R1 and R2 each independently represents halogen, alkyl, alkoxy, nitro or cyano, which comprises allowing a halogenating agent to react with a compound of the formula (I): wherein Alk represents branched alkyl and R1 and R2 are as defined above.