80196-04-9

Basic information

• Product Name: 1-Iodoethyl ethyl carbonate
• Synonyms: 1-IODOETHYL ETHYL CARBONATE;1-Iodoethyl Ethyl Carbonate (JCC-6);BDHXJIRTSWHBPR-UHFFFAOYSA-N
• CAS NO: 80196-04-9
• Molecular Formula: C₅H₉IO₃
• Molecular Weight: 244.03
• Mol File: 80196-04-9.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 190.4 °C at 760 mmHg
• Flash Point: 69 °C
• Appearance: /
• Density: 1.741 g/cm³
• Vapor Pressure: 0.542mmHg at 25°C
• Refractive Index: 1.506
• CAS DataBase Reference: 1-Iodoethyl ethyl carbonate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Iodoethyl ethyl carbonate(80196-04-9)
• EPA Substance Registry System: 1-Iodoethyl ethyl carbonate(80196-04-9)

Safety Data

• Hazardous Substances Data: 80196-04-9(Hazardous Substances Data)

Usage

General Description

1-Iodoethyl ethyl carbonate is a chemical compound with the formula C5H9IO3. It is a colorless liquid with a fruity odor, and is primarily used in organic synthesis as a reagent for the preparation of various organic compounds. It is commonly utilized in the pharmaceutical industry for the synthesis of various drugs and pharmaceutical intermediates. 1-Iodoethyl ethyl carbonate is also employed as a solvent in some chemical reactions and is considered to be a versatile building block in organic chemistry due to its ability to undergo various chemical transformations. 1-Iodoethyl ethyl carbonate is a hazardous substance and should be handled with caution.

InChI:InChI=1/C5H9IO3/c1-3-8-5(7)9-4(2)6/h4H,3H2,1-2H3

Upstream product

• 50893-36-2 1-Chloroethyl ethyl carbonate 

Downstream Products

• 82619-01-0 1-(ethoxycarbonyloxy)ethyl (6R,7R)-7-[(Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetamido]-3-(methoxymethyl)-3-cephem-4-carboxylate 
• 210988-78-6 2-Butyl-5-[methyl-(3-methyl-but-2-enoyl)-amino]-3-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid 1-ethoxycarbonyloxy-ethyl ester 
• 204516-45-0 1-ethoxycarbonyloxyethyl 2,7-diethyl-5-[[2'-(N-triphenylmethyl-tetrazol-5-yl)biphenyl-4-yl]methyl]-5H-pyrazolo[1,5-b][1,2,4]triazole-6-carboxylate 
• 194995-42-1 (4R,5S,6S)-6-((R)-1-Hydroxy-ethyl)-4-methyl-3-{(2R,3R)-2-[(4-nitro-benzyloxycarbonylamino)-methyl]-tetrahydro-furan-3-ylsulfanyl}-7-oxo-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 1-ethoxycarbonyloxy-ethyl ester 

Relevant articles and documents

Synthesis and characterization of novel analogues of cefpodoxime proxetil

The present work describes the origin, identification, synthesis, characterization and control of four novel analogues of cefpodoxime proxetil, which are ethyl, methyl, propyl and N-propyl analogues of cefpodoxime proxetil.

3,3-DISUBSTITUTED-1-HYDROXYTRIAZ-1-ENE 2-OXIDES AND WOUND-HEALING COMPOSITIONS USING THEM

Esters, carbonates and imides of 3,3-disubstituted-1-hydroxytriaz-1-ene 2-oxides of the formula I are disclosed. The compounds release nitric oxide (NO) under physiologic conditions, and pharmaceutical compositions containing them are useful to aid in wound healing.

N-SUBSTITUTED-CYCLIC AMINO DERIVATIVE

The present invention provides a compound of formula (I): wherein R1a is optionally substituted C1-6 alkyl, etc.; R1m is hydrogen atom, etc.; G1, G2, G3 and G4 are (i), etc. ((i) G1 is -N(R1b)-, G2 is -CO-, G3 is -C(R1c)(R1d)-, and G4 is oxygen, etc.); R1b is optionally substituted C1-6 alkyl, etc.; R1c and R1d are each independently optionally substituted C1-6 alkyl, etc.; R2 is optionally substituted C1-6 alkyl, etc.; R3a, R3b, R3c, and R3d are each independently a group: -A-B (A is a single bond, etc., B is hydrogen atom, etc.), etc.; n is 1, etc.; R5 is C1-4 alkoxycarbonyl, etc., or a pharmaceutically acceptable salt thereof, which is useful as a renin inhibitor.