97816-89-2

Basic information

• Product Name: N,N,N'-Trimethyl-N'-thioethylethylene Diamine
• Synonyms: N,N,N'-Trimethyl-N'-thioethylethylene Diamine;2-[[2-(DiMethylaMino)ethyl]MethylaMino]ethanethiol
• CAS NO: 97816-89-2
• Molecular Formula: C7H16N2S
• Molecular Weight: 160.28034
• Product Categories: Aliphatics;Amines;Sulfur & Selenium Compounds
• Mol File: 97816-89-2.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N,N,N'-Trimethyl-N'-thioethylethylene Diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N,N'-Trimethyl-N'-thioethylethylene Diamine(97816-89-2)
• EPA Substance Registry System: N,N,N'-Trimethyl-N'-thioethylethylene Diamine(97816-89-2)

Safety Data

• Hazardous Substances Data: 97816-89-2(Hazardous Substances Data)

Usage

Uses

An intermediate of Synergistin. Antibacterial.

Upstream product

• 5628-96-6 ethyl 2-mercaptoethyl carbonate 
• 142-25-6 N,N',N'-trimethylenediamine 

Relevant articles and documents

Synergistine derivatives and their preparation

The invention provides new synergistine derivatives of the formula: STR1 in which Y=H or N(CH3)2 and R represents: (a) H or OH, (b) a radical of the formula NR1 R2, in which R1 and R2 =H, phenyl or pyridyl (optionally substituted by dialkylamino (1 to 4 C), alkyl (1 to 10 C) [optionally substituted by OH, SH, COOH, anilino, or alkylamino or dialkylamino of which at least one of the alkyl parts is substituted by OH, SH, COOH or anilino 9 , alkenyl (3 or 4 C) or alkynyl (3 or 4 C), or alternatively R1 and R2 together form a heterocycle optionally containing another heteroatom such as O, S or N (optionally substituted by alkyl), or (c) a halogen atom, a trimethylsilyloxy or dialkylphosphoryloxy radical or a radical --OSO2 R3 or --OCOR4, R3 being alkyl, trifluoromethyl, trichloromethyl or optionally substituted phenyl and R4 being defined in the same way as R3 or being an acylalkyl, alkoxycarbonylalkyl or alkoxy radical, and also their salts and their preparation. These products are useful as intermediates in the synthesis of anti-bacterial synergistine derivatives.