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(R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde

(R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde - CAS 15186-48-8

Name: (R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog:	BB010726
Product Name:	(R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde
CAS:	15186-48-8
Synonyms:	(4R)-2,2-dimethyl-1,3-dioxolane-4-carbaldehyde

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Computed Properties

IUPAC Name:	(4R)-2,2-dimethyl-1,3-dioxolane-4-carbaldehyde
Description:	(R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde (CAS# 15186-48-8 ) is a useful research chemical.
Molecular Weight:	130.14
Molecular Formula:	C6H10O3
Canonical SMILES:	CC1(OCC(O1)C=O)C
InChI:	InChI=1S/C6H10O3/c1-6(2)8-4-5(3-7)9-6/h3,5H,4H2,1-2H3/t5-/m0/s1
InChI Key:	YSGPYVWACGYQDJ-YFKPBYRVSA-N
Boiling Point:	72-74°C at 30 Torr
Density:	1.123±0.06 g/cm3
MDL:	MFCD00269682
LogP:	0.33680

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Related Functional Groups

Carbonyl Compounds

[1427004-19-0]C34H39N3O10
DBCO-PEG4-NHS ester
[1383427-98-2]C7H13ClN2O2
(S)-Hexahydropyrazino[2,1-c][1,4]oxazin-4(3H)-one hydrochloride
[959574-98-2]C11H10N2O2
(3-Phenyl-1H-pyrazol-1-yl)acetic acid
[70199-62-1]C8H10ClNO
(4-Pyridyl)acetone Hydrochloride
[1018141-88-2]C17H14N4O2
1-(2-Cyanoethyl)-3-methyl-6-phenyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid
[1006443-01-1]C9H6N4O4
1-(5-Nitropyridin-2-yl)-1H-pyrazole-3-carboxylic acid

GHS Hazard Statement:	H227 (50%): Combustible liquid [Warning Flammable liquids]
Precautionary Statement:	P210, P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P403+P235, P405, and P501
Signal Word:	Warning

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PMID	Publication Date	Title	Journal
21614389	20110821	Ring-closing metathesis (RCM) based synthesis of the macrolactone core of amphidinolactone A	Organic & biomolecular chemistry
20878806	20101122	Metal-catalyzed cycloetherification reactions of β,γ- and γ,δ-allendiols: chemo-, regio-, and stereocontrol in the synthesis of oxacycles	Chemistry (Weinheim an der Bergstrasse, Germany)
20307979	20100415	Synthesis and bioluminescence-inducing properties of autoinducer (S)-4,5-dihydroxypentane-2,3-dione and its enantiomer	Bioorganic & medicinal chemistry letters
20237688	20100407	Asymmetric total synthesis of 1-deoxy-7,8-di-epi-castanospermine	Organic & biomolecular chemistry
19630430	20090820	A sequential indium-mediated aldehyde allylation/palladium-catalyzed cross-coupling reaction in the synthesis of 2-deoxy-beta-C-aryl glycosides	Organic letters

Complexity:	120
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	1
Defined Bond Stereocenter Count:	0
Exact Mass:	130.062994177
Formal Charge:	0
Heavy Atom Count:	9
Hydrogen Bond Acceptor Count:	3
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	130.062994177
Rotatable Bond Count:	1
Topological Polar Surface Area:	35.5 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	0