64743-45-9

Basic information

• Product Name: carbomethoxymethanethiolate
• Synonyms: carbomethoxymethanethiolate
• CAS NO: 64743-45-9
• Molecular Weight: 105.138
• Mol File: 64743-45-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: carbomethoxymethanethiolate(CAS DataBase Reference)
• NIST Chemistry Reference: carbomethoxymethanethiolate(64743-45-9)
• EPA Substance Registry System: carbomethoxymethanethiolate(64743-45-9)

Safety Data

• Hazardous Substances Data: 64743-45-9(Hazardous Substances Data)

Upstream product

• 122801-33-6 C₁₈H₁₈NO₅S^(1-) 

Downstream Products

• 122801-33-6 C₁₈H₁₈NO₅S^(1-) 
• 619-31-8 N,N-dimethyl-3-nitroaniline 
• 61677-76-7 [(methoxymethyl)thio]acetic acid methyl ester 
• 103999-21-9 C₈H₁₀NO₂S^(1-) 
• 166667-91-0 methyl S-nitrosomercaptoacetate 

Relevant articles and documents

Unraveling structure-reactivity relationships in SNV reactions: Kinetics of the reactions of methoxybenzylidenemalononitrile, 2-(methylthiobenzylidene)- 1,3-indandione, 2-(benzylthiobenzylidene)-1,3-indandione, and methyl β-methylthio-α-nitroci

The kinetics of the title reactions were determined in 50% DMSO-50% water (v/v) at 20 °C; n-BuS-, HOCH2CH2S-, and MeO2CCH2S- were used as thiolate ions. The reactions with the th

Lifetimes of iminium ions in aqueous solution

Iminium cations have been generated in aqueous solution from the solvolysis of anilinothioethers ArN-(CH3)CH2SR at 25 °C. Common ion inhibition of the solvolysis of anilinothioethers was observed when the thiolate anion leaving group

Kinetics of reactions of thiolate ions with α-nitro β-substituted stilbenes in 50% Me2SO-50% water. Observation of the intermediate in nucleophilic vinylic substitution reactions

The kinetics of reactions of the type Ph(LG)C=CPh(NO2) + RS- →Ph(RS)C=CPh(NO2) + LG- were measured in 50% Me2SO-50% water (v/v) at 20 °C. Results on the following leaving group/nucleophile combination