(4S,5S)-2,2-Dimethyl-α,α,α',α'-tetraphenyldioxolane-4,5-dimethanol, 98%

Name: (4S,5S)-2,2-Dimethyl-α,α,α',α'-tetraphenyldioxolane-4,5-dimethanol, 98% | 93379-49-8
Brand: J&K Chemical
SKU: JK168185_5_G
Price: 180.5 USD
Availability: InStock

Cat. No JK168185_5_G

Vendor: J&K Chemical

Product Information

Product Name

(4S,5S)-2,2-Dimethyl-α,α,α',α'-tetraphenyldioxolane-4,5-dimethanol, 98%

Brand Name

J&K

Product Number

168185

CAS

93379-49-8

Molecular Formula

C31H30O4

Molecular Weight

466.57

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

(+)-2,3-O-Isopropylidene-1,1,4,4-tetraphenyl-D-threitol
(+)-trans-α,α′-(2,2-Dimethyl-1,3-dioxolane-4,5-diyl)bis(diphenylmethanol)

PubChem CID

9852051

IUPAC Name

(4S,5S)-5-hydroxy(diphenyl)methyl-2,2-dimethyl-1,3-dioxolan-4-yl-diphenylmethanol

InChI Key

OWVIRVJQDVCGQX-NSOVKSMOSA-N

SMILES

CC1(OC@@H(C@H(O1)C(C2=CC=CC=C2)(C3=CC=CC=C3)O)C(C4=CC=CC=C4)(C5=CC=CC=C5)O)C

Properties

Melting Point

193-196

Optical Activity

+65° to +69° (C=1, chloroform)

Safety Information

Storage Condition

Freezer -20℃

References Data Source From Pubchem

First-row transition metal for isocyanide-involving multicomponent reactions (IMCR)

Publication Name: Molecular Diversity

Publication Date: 2022-12-20

DOI: 10.1007/s11030-022-10583-6

Synthesis of (–)-Spicigerolide

Publication Name: Synfacts

Publication Date: 2009-08-21

DOI: 10.1055/s-0029-1217620

The Passerini Reaction: Synthesis of α-Acyloxycarboxamides by the Three-Component Coupling of an Isocyanide, a Carbonyl Compound, and a Carboxylic Acid

Publication Name: Science of Synthesis

Publication Date: 2004

Massive Parallel Catalyst Screening: Toward Asymmetric MCRs

Publication Name: Organic Letters

Publication Date: 2003-10-01

DOI: 10.1021/ol035010u

Asymmetric alkylation catalyzed by chiral alkali metal alkoxides of TADDOL. Synthesis of α-methyl amino acids

Publication Name: Russian Chemical Bulletin

Publication Date: 1999-05

DOI: 10.1007/bf02494637

(4S,5S)-2,2-Dimethyl-α,α,α',α'-tetraphenyldioxolane-4,5-dimethanol, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

First-row transition metal for isocyanide-involving multicomponent reactions (IMCR)

Synthesis of (–)-Spicigerolide

The Passerini Reaction: Synthesis of α-Acyloxycarboxamides by the Three-Component Coupling of an Isocyanide, a Carbonyl Compound, and a Carboxylic Acid

Massive Parallel Catalyst Screening: Toward Asymmetric MCRs

Asymmetric alkylation catalyzed by chiral alkali metal alkoxides of TADDOL. Synthesis of α-methyl amino acids