192439-46-6

Basic information

• Product Name: N-[3-methyl-5-[(2-phenylsulfanylthiazol-5-yl)methyl]-1,3,5-oxadiazinan-4-ylidene]nitramide
• CAS NO: 192439-46-6
• Molecular Formula: C₁₄H₁₅N₅O₃S₂
• Molecular Weight: 365.43
• Mol File: 192439-46-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 576.5°C at 760 mmHg
• Flash Point: 302.5°C
• Density: 1.5g/cm³
• Vapor Pressure: 2.72E-13mmHg at 25°C
• Refractive Index: 1.717
• CAS DataBase Reference: N-[3-methyl-5-[(2-phenylsulfanylthiazol-5-yl)methyl]-1,3,5-oxadiazinan-4-ylidene]nitramide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[3-methyl-5-[(2-phenylsulfanylthiazol-5-yl)methyl]-1,3,5-oxadiazinan-4-ylidene]nitramide(192439-46-6)
• EPA Substance Registry System: N-[3-methyl-5-[(2-phenylsulfanylthiazol-5-yl)methyl]-1,3,5-oxadiazinan-4-ylidene]nitramide(192439-46-6)

Safety Data

• Hazardous Substances Data: 192439-46-6(Hazardous Substances Data)

Usage

General Description

N-[3-methyl-5-[(2-phenylsulfanylthiazol-5-yl)methyl]-1,3,5-oxadiazinan-4-ylidene]nitramide is a chemical compound with a complex and lengthy name, representing a nitramide derivative. It contains a nitramide functional group, which consists of a nitro group (-NO2) attached to an amine group (-NH2). The compound also features a thiazole ring, an oxadiazinan ring, and a phenylsulfanyl group, giving it a diverse and unique molecular structure. This chemical may have potential applications in fields such as pharmaceuticals, agrochemicals, or materials science, but further research and testing would be necessary to determine its specific uses and properties.

Upstream product

• 153719-38-1 3,6-dihydro-3-methyl-N-nitro-2H-1,3,5-oxadiazin-4-amine 
• 153719-38-1 3-methyl-4-nitroimino-perhydro-1,3,5-oxadiazine 
• 36273-11-7 1-(chloromethyl)-4-aza-1-azoniabicyclo[2.2.2]octane chloride 

Relevant articles and documents

Process for the preparation of thiazole derivatives

The Invention relates to a process for the preparation of a compound of the formula wherein Q, Y, Z, R1, R2, R3, R4and R5are as defined in the specification, which comprises a) reacting a compound of the formula ?with a halogenating agent to form a compound of the formula b) converting a compound of formula (II) by means of a halogenating agent into a compound of the formula ?optionally c) converting the compound of formula (IV) into a compound of formula (III); d) converting a compound of formula (III) by means of a compound of the formula e) converting a compound (IV) by means of a compound (V) into a compound (VI); and f) converting a compound (VI) by means of a chlorinating agent into a compound (I); a compound (IV); to a process for the preparation of a compound (III) and to a process for the preparation of a compound (IV).