59490
(4R,5R)-2,2-Dimethyl-α,α,α′,α′-tetra(2-naphthyl)dioxolane-4,5-dimethanol
≥99.0% (sum of enantiomers, HPLC)
Synonym(s):
(−)-2,3-O-Isopropylidene-1,1,4,4-tetra(2-naphthyl)-L-threitol, (−)-DINOL
About This Item
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Assay
≥99.0% (sum of enantiomers, HPLC)
optical activity
[α]20/D −116±2°, c = 1% in ethyl acetate
optical purity
enantiomeric ratio: ≥99.5:0.5 (HPLC)
mp
213-216 °C (lit.)
functional group
ether
hydroxyl
ketal
storage temp.
2-8°C
SMILES string
CC1(C)O[C@H]([C@@H](O1)C(O)(c2ccc3ccccc3c2)c4ccc5ccccc5c4)C(O)(c6ccc7ccccc7c6)c8ccc9ccccc9c8
InChI
1S/C47H38O4/c1-45(2)50-43(46(48,39-23-19-31-11-3-7-15-35(31)27-39)40-24-20-32-12-4-8-16-36(32)28-40)44(51-45)47(49,41-25-21-33-13-5-9-17-37(33)29-41)42-26-22-34-14-6-10-18-38(34)30-42/h3-30,43-44,48-49H,1-2H3/t43-,44-/m1/s1
InChI key
QWADMRIAKWGVBF-NDOUMJCMSA-N
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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Articles
TADDOLs demonstrate versatility in metal-catalyzed asymmetric reactions and as Brønsted acid organocatalysts in hetero-Diels–Alder reactions.
TADDOLs demonstrate versatility in metal-catalyzed asymmetric reactions and as Brønsted acid organocatalysts in hetero-Diels–Alder reactions.
TADDOLs demonstrate versatility in metal-catalyzed asymmetric reactions and as Brønsted acid organocatalysts in hetero-Diels–Alder reactions.
TADDOLs demonstrate versatility in metal-catalyzed asymmetric reactions and as Brønsted acid organocatalysts in hetero-Diels–Alder reactions.
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