438960
(R)-(+)-3-Benzyloxy-1,2-propanediol
99%
Synonym(s):
(R)-Glycerol 1-benzyl ether, 3-O-Benzyl-sn-glycerol, 3-Benzyl-sn-glycerol
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
C6H5CH2OCH2CH(OH)CH2OH
CAS Number:
Molecular Weight:
182.22
UNSPSC Code:
12352201
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2048922
Product Name
(R)-(+)-3-Benzyloxy-1,2-propanediol, 99%
InChI
1S/C10H14O3/c11-6-10(12)8-13-7-9-4-2-1-3-5-9/h1-5,10-12H,6-8H2/t10-/m1/s1
SMILES string
OC[C@@H](O)COCc1ccccc1
InChI key
LWCIBYRXSHRIAP-SNVBAGLBSA-N
assay
99%
form
solid
optical activity
[α]20/D +5.5°, c = 20 in chloroform
mp
25-29 °C (lit.)
storage temp.
2-8°C
Quality Level
Application
Employed in the synthesis of a cyclopropyl chiron used in the preparation of 2,3-methanoamino acids. Chiral building block in the synthesis of petrosynes and biologically important phospholipid analogs.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
T N Wheeler et al.
Journal of medicinal chemistry, 37(24), 4118-4129 (1994-11-25)
The substrate specificity at the active site of recombinant human synovial fluid phospholipase A2 (hs-PLA2) was investigated by the preparation of a series of short-chain phospholipid analogs and measurement of their enzymatic hydrolysis at concentrations well below the critical micelle
Burgess, K. et al.
The Journal of Organic Chemistry, 58, 3767-3767 (1993)
Iguchi, K. et al.
The Journal of Organic Chemistry, 58, 5690-5690 (1993)
S.F. Martin et al.
The Journal of Organic Chemistry, 59, 4805-4805 (1994)
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