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DIVINYL ETHER

Divinyl ether

Chemical compound

Divinyl ether is the organic compound with the formula O(CH=CH2)2. It is a colorless, volatile liquid that has mainly been of interest as an inhalation

Divinyl ether

Divinyl_ether

Vinyl ether

Topics referred to by the same term

Vinyl ether may refer to: Any enol ether Divinyl ether, a volatile chemical compound once used as an anesthetic This disambiguation page lists articles

Vinyl ether

Vinyl_ether

Bis(chloroethyl) ether

Chemical compound

gives divinyl ether, an anesthetic: O(CH2CH2Cl)2 + 2 KOH → O(CH=CH2)2 + 2 KCl + 2 H2O The LD50 is 74 mg/kg (oral, rat). Bis(chloroethyl) ether is considered

Bis(chloroethyl) ether

Bis(chloroethyl)_ether

Diethyl ether

Organic chemical compound

Diethyl ether, or simply ether (abbreviated as eth. or Et2O) is an organic compound with the chemical formula (CH3CH2)2O, belonging to the ether class.

Diethyl ether

Diethyl_ether

Methyl vinyl ether

Chemical compound

toxicity of vinyl ethers has been heavily investigated because divinyl ether has been used as an anesthetic. The acute LD50 for methyl vinyl ether is greater

Methyl vinyl ether

Methyl_vinyl_ether

Divinylether fatty acids

Class of chemical compounds

known to serve as substrates for a divinyl ether synthase which produces divinyl ether fatty acids. Divinyl ethers were detected only within the plant kingdom

Divinylether fatty acids

Divinylether_fatty_acids

Inhalational anesthetic

Volatile or gaseous anesthetic compound delivered by inhalation

Acetylene Chloroethane (ethyl chloride) Chloroform Cyclopropane Diethyl ether Divinyl ether Enflurane Ethylene Fluroxene Halothane (still widely used in the

Inhalational anesthetic

Inhalational_anesthetic

Colneleate synthase

Enzyme

Colneleate synthase (EC 4.2.1.121, 9-divinyl ether synthase, 9-DES, CYP74D, CYP74D1, CYP74 cytochrome P-450, DES1) is an enzyme with systematic name (8E)-9-((1E

Colneleate synthase

Colneleate_synthase

Karl Koller (ophthalmologist)

Austrian ophthalmologist (1857–1944)

Leake recovered his sight and, as an adult, discovered the anaesthetic divinyl ether. Sigmund Freud reportedly nicknamed Koller "Coca Koller" because of

Karl Koller (ophthalmologist)

Karl_Koller_(ophthalmologist)

Divinyl sulfide

Chemical compound

Divinyl sulfide is the organosulfur compound with the formula S(CH=CH2)2. A colorless liquid with a faint odor, it is found in some species of Allium

Divinyl sulfide

Divinyl_sulfide

C4H6O

Index of chemical compounds with the same molecular formula

Crotonaldehyde Cyclobutanone Dihydrofurans 2,3-Dihydrofuran 2,5-Dihydrofuran Divinyl ether Methacrolein Methyl vinyl ketone This set index page lists chemical

C4H6O

Bis(2-chloroethyl)sulfide

Chemical compound formerly used in warfare

+ H2SO4 Bis(2-chloroethyl)sulfide reacts with sodium hydroxide, giving divinyl sulfide: (ClC2H4)2S + 2 NaOH → (CH2=CH)2S + 2 H2O + 2 NaCl Sodium ethoxide

Bis(2-chloroethyl)sulfide

Furan

Heterocyclic organic compound,

temperature. It is soluble in common organic solvents, including alcohol, ether, and acetone, and is slightly soluble in water. Its odor is strong and chloroform-like

Furan

List of UN numbers 1101 to 1200

Numbers, classes, and proper shipping names allocated to dangerous goods

3 Dimethyl sulfide UN 1165 3 Dioxane UN 1166 3 Dioxolane UN 1167 3 Divinyl ether, inhibited UN 1168 ? (UN No. no longer in use) Driers or varnish, liquid

List of UN numbers 1101 to 1200

List_of_UN_numbers_1101_to_1200

Karstedt's catalyst

Chemical compound

Karstedt's catalyst is an organoplatinum compound derived from divinyl-containing disiloxane. This coordination complex is widely used in hydrosilylation

Karstedt's catalyst

Karstedt's_catalyst

Chauncey D. Leake

American pharmacologist, medical historian and ethicist

Wisconsin in pharmacology and physiology. Leake discovered the anesthetic divinyl ether. He authored over 400 publications. One of his publications was a translation

Chauncey D. Leake

Chauncey_D._Leake

Fluroxene

Chemical compound

compound responsible for some of the toxicity seen with fluroxene use. Divinyl ether Thiomethoxyflurane Stoelting RK, Hillier SC (11 January 2012). "Inhaled

Fluroxene

Chlorophyll c

Chemical compound

reductase (elaborating on the promiscuous behavior of ferredoxin-type 3,8-divinyl chlorophyllide reductase) could also convert Chl c2 into Chl c1. The two

Chlorophyll c

Chlorophyll_c

Nazarov cyclization

Chemical reaction used in organic chemistry

originally described, the Nazarov cyclization involves the activation of a divinyl ketone using a stoichiometric Lewis acid or protic acid promoter. The key

Nazarov cyclization

Nazarov_cyclization

3,9-Divinyl-2,4,8,10-tetraoxaspiro(5.5)undecane

Chemical compound

3,9-Divinyl-2,4,8,10-tetraoxaspiro[5.5]undecane (DVTOSU) is a bicyclic organic molecule having a central quaternary carbon atom (a spiro atom) with which

3,9-Divinyl-2,4,8,10-tetraoxaspiro(5.5)undecane

Hydroperoxide lyase

Class of enzymes

PMID 11828481. S2CID 29327220. Grechkin AN (2002). "Hydroperoxide lyase and divinyl ether synthase". Prostaglandins & Other Lipid Mediators. 68–69: 457–70. doi:10

Hydroperoxide lyase

Hydroperoxide_lyase

Vinyl group

Chemical group (–CH=CH2)

vinyl groups. (A styrenic crosslinker with two vinyl groups is called divinyl benzene.) Vinyl groups can polymerize with the aid of a radical initiator

Vinyl group

Vinyl_group

Samuel Gelfan

Anesthetic Action of Divinyl Oxide on Humans". Journal of Pharmacology and Experimental Therapeutics. 47 (1): 1–3. (See divinyl ether.) Adrian, E. D.; Gelfan

Samuel Gelfan

Samuel_Gelfan

Hyaluronic acid

Physiological molecule and therapeutic drug

4-diepoxybutane, as well as other crosslinkers like divinyl sulfone (DVS) and ethylene sulfide. These ether linkages are stable to hydrolysis, providing long

Hyaluronic acid

Hyaluronic_acid

Butadiene

Chemical compound

Names Preferred IUPAC name Buta-1,3-diene Other names Biethylene Erythrene Divinyl Vinylethylene Bivinyl Butadiene Identifiers CAS Number 106-99-0 Y 3D model

Butadiene

Divinylbenzene

Organic compound, C6H4(CH=CH2)2

water 0.005% (20°C) Solubility in other solvents Soluble in ethanol and ether Vapor pressure 0.7 mmHg (20°C) Hazards Flash point 76 °C (169 °F; 349 K)

Divinylbenzene

Acetylene

Hydrocarbon compound (HC≡CH)

commercial grades usually have a marked odor due to impurities such as divinyl sulfide and phosphine. As an alkyne, acetylene is unsaturated because its

Acetylene

List of compounds with carbon number 4

C4H6O2 isocrotonic acid 503-64-0 C4H6O2S diacetyl sulfide 3232-39-1 C4H6O2S divinyl sulfone 77-77-0 C4H6O3 acetic anhydride 108-24-7 C4H6O3 propylene carbonate

List of compounds with carbon number 4

List_of_compounds_with_carbon_number_4

Sulfone

Organosulfur compound of the form >S(=O)2

Fernando; Lopez-Jaramillo, F. Javier; Ortega-Muñoz, Mariano (2021). "Divinyl Sulfone". Encyclopedia of Reagents for Organic Synthesis. pp. 1–8. doi:10

Sulfone

Cyclic compound

Molecule with a ring of bonded atoms

the Nazarov cyclization reaction, originally being the cyclization of a divinyl ketone; various radical cyclizations; ring-closing metathesis reactions

Cyclic compound

Cyclic_compound

List of compounds with carbon number 10

ethylsyringol 29515–37–5 C10H14O3 mephenesin 59–47–2 C10H14O4 adipic acid divinyl ester 4074–90–2 C10H14O4 diallyl succinate 925–16–6 C10H14S butylthiobenzene

List of compounds with carbon number 10

List_of_compounds_with_carbon_number_10

List of EC numbers (EC 1)

reductase EC 1.3.1.74: 2-alkenal reductase [NAD(P)+] EC 1.3.1.75: 3,8-divinyl protochlorophyllide a 8-vinyl-reductase (NADPH) EC 1.3.1.76: precorrin-2

List of EC numbers (EC 1)

List_of_EC_numbers_(EC_1)