50594-94-0

Usage

Uses

Used in Organic Synthesis:
Methanol, chloro-, carbonate (2:1) is used as a reagent in organic synthesis for various chemical reactions, due to its ability to act as a solvent and its reactivity with other compounds.
Used in Industrial Processes:
Methanol, chloro-, carbonate (2:1) is used as a solvent in various industrial processes, such as the production of pharmaceuticals, agrochemicals, and other chemicals, due to its ability to dissolve a wide range of substances and facilitate chemical reactions.
Used in Environmental Remediation:
Methanol, chloro-, carbonate (2:1) can be used in the remediation of contaminated water and soil, as it can help break down and remove pollutants, although its use in this context must be carefully managed to prevent further harm to the environment.

Upstream product

• 22128-62-7 carbonochloridic acid, chloromethyl ester 
• 58-22-0 testosterone 
• 616-38-6 carbonic acid dimethyl ester 

Downstream Products

• 215927-11-0 Acetic acid (2R,3S,5R)-2-acetoxymethyl-5-(3-chloromethoxycarbonyloxymethyl-5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 
• 143588-03-8 1-t-butoxycarbonyl-4-hydroxy-3-(N-methoxycarbonyl-N-methyl)aminopyrrolidine 
• 84756-61-6 iodomethyl carbonate 

Relevant academic research and scientific papers

Compositions and methods for enhanced drug delivery

The present invention relates to methods of delivering pharmaceutical agents across membranes, including the skin layer or mucosal membranes of a patient. A pharmaceutical agent is covalently bonded to a chemical modifier, via a physiologically cleavable bond, such that the membrane transport and delivery of the agent is enhanced.

Contrast agents comprising gas-containing or gas-generating polymer microparticles or microballoons

Contrast agents comprising gas-containing or gas-generating polymer microparticles and/or microballoons, in which the polymer is a biodegradable polymer containing units of formula (wherein R1 and R2 each represent hydrogen or a carbon-attached monovalent organic group or together form a carbon-attached divalent organic group, and m and n are each independently zero or one) may be used in diagnostic applications such as ultrasound and MR imaging.

Cleavage of carbon-sulfur bonds in the synthesis of α-haloalkyl carbonates

α-Chloroalkyl and α-bromoalkyl carbonates have been prepared by cleavage of α-arylthioalkyl carbonates with sulfuryl chloride or bromine, respectively. The α-arylthioalkyl carbonates are prepared by reaction of the hemithioacetal 1 with chloroformates or by a destannylative tin-Pummerer rearrangement of α-stannyl sulfoxides. Acta Chemica Scandinavica 1996.