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Merck
CN

218855

9-氯-9-苯基氧杂蒽

97%

别名:

Pixyl chloride

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关于此项目

经验公式(希尔记法):
C19H13ClO
化学文摘社编号:
分子量:
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.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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分析证书(COA)

Lot/Batch Number

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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 pixyl (Px) group: a novel photocleavable protecting group for primary alcohols.
Misetic A and Boyd MK.
Tetrahedron Letters, 39(13), 1653-1656 (1998)
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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