Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C19H13ClO
CAS Number:
Molecular Weight:
292.76
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
255-857-5
Beilstein/REAXYS Number:
237712
MDL number:
Assay:
97%
Form:
solid
InChI key
HTGMODSTGYKJDG-UHFFFAOYSA-N
InChI
1S/C19H13ClO/c20-19(14-8-2-1-3-9-14)15-10-4-6-12-17(15)21-18-13-7-5-11-16(18)19/h1-13H
SMILES string
ClC2(c1ccccc1)c3ccccc3Oc4ccccc24
assay
97%
form
solid
solubility
chloroform: soluble 25 mg/mL, clear, yellow to orange
Application
9-Chloro-9-phenylxanthene was used in the preparation of (1S,5S,6R,8S)-6-[(allyloxycarbonyl)oxy]-5-(trifluoroacetamido)-8-[9′-(9′-phenylxanthenyl)oxy]-2-oxabicyclo(3.2.1)octane.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
新产品
This item has
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.
The pixyl (Px) group: a novel photocleavable protecting group for primary alcohols.
Misetic A and Boyd MK.
Tetrahedron Letters, 39(13), 1653-1656 (1998)
I Pompizi et al.
Nucleic acids research, 28(14), 2702-2708 (2000-07-25)
The synthesis and incorporation into oligodeoxy-nucleotides of two novel, conformationally restricted abasic (AB) site analogs are described. The stability of oligonucleotide 18mer duplexes containing one such AB site opposite any of the four natural DNA bases was investigated by UV
The 9-phenylxanthen-9-yl protecting group.
Chattopadhyaya JB and Reese CB.
Journal of the Chemical Society. Chemical Communications, 15, 639-640 (1978)
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