Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

254827

Sigma-Aldrich

(+)-Noe-lactol dimer

≥99%

Synonym(s):

(+)-MBF-OH dimer, (+)-Noe’s reagent, (2R,3aS,4R,7aS)-Octahydro-7,8,8-trimethyl-4,7-methanobenzofuran-2-yl ether, Bis[(2R,3aS,4R,7aS)octahydro-7,8,8-trimethyl-4,7-methanobenzofuran-2-yl] ether

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C24H38O3
CAS Number:
Molecular Weight:
374.56
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

Assay

≥99%

form

solid

optical activity

[α]21/D +199.1°, c = 2.25 in THF

mp

150-151 °C (lit.)

SMILES string

CC1(C)[C@@H]2CC[C@@]1(C)[C@H]3O[C@@H](C[C@@H]23)O[C@@H]4C[C@H]5[C@H]6CC[C@@](C)([C@H]5O4)C6(C)C

InChI

1S/C24H38O3/c1-21(2)15-7-9-23(21,5)19-13(15)11-17(26-19)25-18-12-14-16-8-10-24(6,20(14)27-18)22(16,3)4/h13-20H,7-12H2,1-6H3/t13-,14-,15+,16+,17-,18-,19-,20-,23-,24-/m0/s1

InChI key

VUDXCBLBKXFCNA-VFQSMPPFSA-N

Application

(+)-Noe-lactol dimer can be used to prepare:
  • Axially chiral isoquinoline derivatives by reacting with pyridinium p-toluenesulfonate.
  • Halofuginone lactate.

Legal Information

Noe-Lactol is a trademark of Sigma-Aldrich Co. LLC

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Enantioselective synthesis of axially chiral 1-(1-naphthyl) isoquinolines and 2-(1-naphthyl) pyridines through sulfoxide ligand coupling reactions
Baker RW, et al.
Tetrahedron, 61(15), 3733-3743 (2005)
(2R, 3S)-(+)-and (2S, 3R)-(−)-Halofuginone lactate: Synthesis, absolute configuration, and activity against Cryptosporidium parvum
Linder MR, et al.
Bioorganic & medicinal chemistry letters, 17(15), 4140-4143 (2007)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service