Divinyloxyethane

Product Information

Molecular Formula:
C6H10O2
Molecular Weight:
114.14
Description
Divinyloxyethane is a pivotal chemical entity in the realm of biomedical applications and is extensively employed for drug delivery system design and diverse ailment treatments. Its multifaceted nature enables its utilization as a fundamental constituent in the synthesis of groundbreaking pharmaceutical compounds and polymers. Through its extraordinary chemical attributes, Divinyloxyethane assumes a paramount function in propelling pharmaceutical exploration and enhancing therapeutic results.
Synonyms
3,4-dihydroxy-5-hexadiene; divinyloxyethane(divinylglycol); DVG; DIVINYLOXYETHANE; DIVINYLETHYLENE GLYCOL; DIVINYL GLYCOL
IUPAC Name
hexa-1,5-diene-3,4-diol
Canonical SMILES
C=CC(C(C=C)O)O
InChI
InChI=1S/C6H10O2/c1-3-5(7)6(8)4-2/h3-8H,1-2H2
InChI Key
KUQWZSZYIQGTHT-UHFFFAOYSA-N
Boiling Point
125ºC (45 mmHg)
Melting Point
14-16ºC
Flash Point
199.4 ℃F - closed cup
Purity
BP 94-96deg/10mm
Density
1.02
Appearance
Light yellow oily liquid
Storage
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. Store protected from light.
Refractive Index
n20/D 1.479 (lit.)

Safety Information

Hazards
H302:
Harmful if swallowed.
H311:
Toxic in contact with skin.
Precautionary Statement
P264:
Wash thoroughly after handling.
P270:
Do not eat, drink or smoke when using this product.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352+P312:
IF ON SKIN:
Wash with plenty of soap and water.
Call a POISON CENTER or doctor/physician if you feel unwell.
P361+P364:
Take off immediately all contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.

Computed Properties

XLogP3
0.2
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
3
Exact Mass
114.068079557 g/mol
Monoisotopic Mass
114.068079557 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
8
Formal Charge
0
Complexity
76.5
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
2
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114015035-A Multifunctional water reducer polyether, preparation method thereof, mud-resistant polycarboxylate water reducer derived from multifunctional water reducer polyether, and preparation method and application of mud-resistant polycarboxylate water reducer 2021-12-22
CN-114159629-A High-speed preparation method of blood vessel covered stent for emergency treatment of sudden coronary perforation in operation 2021-12-07
CN-113563588-A Hydroxyl-terminated siloxane, silicon polyurethane containing same and preparation method thereof 2021-07-28
CN-113299359-A Clinical data management statistical analysis method for evaluation of calcium polycarbophil tablets based on pharmacokinetics 2021-07-27
CN-113299359-B Clinical data management statistical analysis method for evaluation of calcium polycarbophil tablets based on pharmacokinetics 2021-07-27
CN-215750780-U Three-dimensional object printing device 2021-07-26
CN-113402562-A Preparation method and application of platinum complex 2021-06-11
CN-113416293-A High-tensile-property medical hydrogel and preparation method and application thereof 2021-05-27
CN-113213507-A Method for removing impurity ions in liquid ammonia 2021-05-12
CN-113416292-A Hydrogel capable of loading high-hydrophobicity drugs and preparation method and application thereof 2021-04-30

Literatures

PMID Publication Date Title Journal
21381727 2011-04-01 Desymmetrization of (R,R)-hexa-1,5-diene-3,4-diol via monofunctionalization and rhodium-catalyzed allylic substitution The Journal of organic chemistry
15524428 2004-11-11 Concise total synthesis of (-)-muricatacin by tandem ring-closing/cross metathesis Organic letters
15255735 2004-07-23 Direct preparation of allylic indium(III) reagents from allylic alcohols via a reductive transmetalation of pi-allylnickel(II) with indium(I) iodide The Journal of organic chemistry
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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