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(+)-Taddol
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(+)-Taddol

CAS: 93379-49-8

Ref. 3D-FT38495

1gDiscontinued
2gDiscontinued
5gDiscontinued
10gDiscontinued
25gDiscontinued

Discontinued product. For inquiries about similar products, please fill out our form or email us at .


Product Information

Name:
(+)-Taddol
Synonyms:
  • (+)-4,5-Bis[hydroxy(diphenyl)methyl]-2,2-dimethyl-1,3-dioxolane
  • (+)-Taddol I
  • (+)-trans-A,A-(2,2-dimethyl-1,3-dioxolane-4,5-D
  • (+)-trans-α,α′-(2,2-Dimethyl-1,3-dioxolane-4,5-diyl)bis(diphenylmethanol)
  • (4S,5S)-2,2-Dimethyl-alpha,alpha,alpha,alpha-tetraphenyldioxolane-4,5-dimethanol
  • (4S,5S)-2,2-Dimethyl-α,α,α',α'-tetraphenyldioxolane-4,5-dimethanol
  • (4S,5S)-2,2-Dimethyl-α<sup>4</sup>,α<sup>4</sup>,α<sup>5</sup>,α<sup>5</sup>-tetraphenyl-1,3-dioxolane-4,5-dimethanol
  • (4S,5S)-4,5-Bis(hydroxydiphenylmethyl)-2,2-dimethyl-1,3-dioxolane
  • (4S,5S)-Taddol
  • (S)-Taddol
  • See more synonyms
  • (S,S)-2,2-Dimethyl-α,α,α′,α′-tetraphenyl-1,3-dioxolane-4,5-dimethanol
  • (S,S)-4,5-Bis(diphenylhydroxymethyl)-2,2-dimethyl-1,3-dioxolane
  • (S,S)-Taddol
  • 1,3-Dioxolane-4,5-dimethanol, 2,2-dimethyl-α,α,α′,α′-tetraphenyl-, (4S,5S)-
  • 1,3-Dioxolane-4,5-dimethanol, 2,2-dimethyl-α,α,α′,α′-tetraphenyl-, (4S-trans)-
  • 1,3-Dioxolane-4,5-dimethanol, 2,2-dimethyl-α<sup>4</sup>,α<sup>4</sup>,α<sup>5</sup>,α<sup>5</sup>-tetraphenyl-, (4S,5S)-
  • Bishydroxydiphenylmethyldimethyldioxolane
  • [(4S,5S)-2,2-dimethyl-1,3-dioxolane-4,5-diyl]bis(diphenylmethanol)
  • 1,3-Dioxolane-4,5-dimethanol, 2,2-dimethyl-α4,α4,α5,α5-tetraphenyl-, (4S,5S)-
  • (4S,5S)-2,2-Dimethyl-α4,α4,α5,α5-tetraphenyl-1,3-dioxolane-4,5-dimethanol
Description:

(+)-Taddol is a synthetic compound that is used in the preparation of other compounds. It has been shown to be reactive, and it is typically used in cross-coupling reactions, which involve the formation of new carbon-carbon bonds between two organic molecules. (+)-Taddol is a macrocyclization precursor that can be used for the synthesis of chiral compounds with high stereospecificity. This compound also has been found to have anti-cancer properties. The clinical use of (+)-taddol is as an intermediate for other drugs or as a ligand in metal coordination complexes. Preparative methods include alkylation, which involves the addition of an alkyl group to an organic molecule with the use of a strong base such as NaOH or KOH. Ligands are molecules that bind specifically to metal ions and are often used in chemical reactions. Reaction products from (+)-taddol's preparative method include propargylation, which involves

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Purity:
Min. 95%
MDL:
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EINECS:
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HS code:

Hazard Info

UN Number:
EQ:
Class:
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Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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