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Merck
CN

218855

9-Chloro-9-phenylxanthene

97%

Synonym(s):

Pixyl chloride

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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
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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

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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)

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