456268
(S)-(−)-Glycidyl trityl ether
98%
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About This Item
Empirical Formula (Hill Notation):
C22H20O2
CAS Number:
Molecular Weight:
316.39
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
98%
form
solid
optical activity
[α]20/D −10.5°, c = 1 in chloroform
optical purity
ee: 98% (GLC)
mp
99-102 °C (lit.)
functional group
ether
phenyl
SMILES string
C1O[C@@H]1COC(c2ccccc2)(c3ccccc3)c4ccccc4
InChI
1S/C22H20O2/c1-4-10-18(11-5-1)22(24-17-21-16-23-21,19-12-6-2-7-13-19)20-14-8-3-9-15-20/h1-15,21H,16-17H2/t21-/m0/s1
InChI key
XFSXUCMYFWZRAF-NRFANRHFSA-N
Related Categories
Application
(S)-(-)-Glycidyl trityl ether may be used to prepare N-(p-alkoxy)benzoyl-2-methylindole-4-acetic acid analogs, which are potent prostaglandin D2 (PGD2) receptor antagonists. It may also be used as a starting material in the multi-step synthesis of (-)-actisonitrile.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Discovery of orally active prostaglandin D 2 receptor antagonists.
Torisu K, et al.
Bioorganic & Medicinal Chemistry Letters, 14(19), 4891-4895 (2004)
Discovery of a new class of potent, selective, and orally active prostaglandin D 2 receptor antagonists.
Torisu K, et al.
Bioorganic & Medicinal Chemistry, 12(20), 5361-5378 (2004)
Structure and synthesis of a unique isonitrile lipid isolated from the marine mollusk Actinocyclus papillatus.
Manzo E, et al.
Organic Letters, 13(8), 1897-1899 (2011)
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