Name: Name:(R)-2,2-Dimethyl-1,3-dioxolane-4-carbaldehyde
Brand: Angene
SKU: AG00327I
Rating: 90 (10 reviews)

(R)-2,2-Dimethyl-1,3-dioxolane-4-carbaldehyde

CAS No.:

15186-48-8

Catalog Number:

AG00327I

Molecular Formula:

C6H10O3

Molecular Weight:

130.1418

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Product Description

Catalog Number:

AG00327I

Chemical Name:

(R)-2,2-Dimethyl-1,3-dioxolane-4-carbaldehyde

CAS Number:

15186-48-8

Molecular Formula:

C6H10O3

Molecular Weight:

130.1418

MDL Number:

MFCD00269682

IUPAC Name:

(4R)-2,2-dimethyl-1,3-dioxolane-4-carbaldehyde

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

SMILES:

O=C[C@H]1COC(O1)(C)C

NSC Number:

89869

Properties

Complexity:

120

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

130.063g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

130.143g/mol

Monoisotopic Mass:

130.063g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

35.5A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

Literature

Title	Journal
Ring-closing metathesis (RCM) based synthesis of the macrolactone core of amphidinolactone A.	Organic & biomolecular chemistry 20110821
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) 20101122
Synthesis and bioluminescence-inducing properties of autoinducer (S)-4,5-dihydroxypentane-2,3-dione and its enantiomer.	Bioorganic & medicinal chemistry letters 20100415

Properties