Structure via PubChem · Public domain (PubChem)
паральдегид
Sign in to saveAlso known as Paral, paracetaldehyde, acetaldehyde trimer, paraacetaldehyde, 2,4,6-trimethyl-s-trioxane, 1,3,5-trimethyl-2,4,6-trioxane, Paraldehyde, 2,4,6-trimethyl-1,3,5-trioxane
химическое соединение
In the Vinony graph
Vinony's link graph records 862 inbound references to паральдегид, and connects out to benzodiazepine drug, allopregnanolone and isovaleric acid.
It is catalogued under topics including Acetals, Anticonvulsants and Chembox having GHS data.
Vinony links it to 29 Wikipedia language editions.
Chemical data
- Formula
- C6H12O3
- Molecular weight
- 132.16 g/mol
- IUPAC name
- 2,4,6-trimethyl-1,3,5-trioxane
- SMILES
- CC1OC(OC(O1)C)C
- InChIKey
- SQYNKIJPMDEDEG-UHFFFAOYSA-N
- XLogP
- 0.7
- Polar surface area
- 27.7 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Approved
- Molecule type
- Small molecule
- Indications
- status epilepticus
via ChEMBL · EBI
Research
577 papers- Paraldehyde.Journal of applied toxicology : JAT · 1991
- Paraldehyde acidosis.The American journal of medicine · 1967
- Paraldehyde.The Hospital · 1893
- [Paraldehyde].The Canadian nurse · 1948
- Eclampsia.Clinics in obstetrics and gynaecology · 1982
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Has part
- carbon
- Mass
- 132.078644
- Has use
- medication
Show 10 more facts
- melting point
- 12.6
- chemical formula
- C₆H₁₂O₃
- Commons category
- Paraldehyde
- electric dipole moment
- 1.43
- World Health Organisation international non-proprietary name
- paraldehyde
- canonical SMILES
- CC1OC(OC(O1)C)C
- isomeric SMILES
- C[C@@H]1O[C@@H](OC(O1)C)C
- different from
- paraformaldehyde
- described by source
- Encyclopædia Britannica 11th edition
- boiling point
- 124.35
via Wikidata · CC0
Article · Русский
Паральдегид — органическое соединение, циклический тример ацетальдегида, бесцветная жидкость, растворимая в воде и органических растворителях.
Abstract from DBpedia / Wikipedia · CC BY-SA