368873
9-溴-9-苯基芴
97%
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关于此项目
经验公式（希尔记法）:
C19H13Br
化学文摘社编号:
分子量:
321.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
InChI
1S/C19H13Br/c20-19(14-8-2-1-3-9-14)17-12-6-4-10-15(17)16-11-5-7-13-18(16)19/h1-13H
SMILES string
BrC2(c1ccccc1)c3ccccc3-c4ccccc24
InChI key
HYQXNCDBSALQLB-UHFFFAOYSA-N
assay
97%
mp
99-101 °C (lit.)
functional group
bromo, phenyl
General description
Solvolysis of 9-bromo-9- phenylfluorene has been reported to proceed via limiting SN1 mechanism.
Application
9-Bromo-9-phenylfluorene may be used in the preparation of:
- N-(9-(9-phenylfluorenyl))-L-alaninal
- N-(9-phenylfluoren-9-yl)-L-serine
- 1-hydroxypyrazoles priotected at the oxygen atom
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Solvent and Substituent Effects in the Solvolysis of 9-Aryl-9-bromofluorenes.
Liu K-T and Lin Y-S.
J. Chin. Chem. Soc., 47(1), 71-76 (2000)
Configurational stability of N-protected. alpha.-amino aldehydes.
Lubell WD and Rapoport H.
Journal of the American Chemical Society, 109(1), 236-239 (1987)
Synthesis of 5-substituted 1-hydroxypyrazoles through directed lithiation of 1-(benzyloxy) pyrazole.
Vedso P and Begtrup M.
The Journal of Organic Chemistry, 60(16), 4995-4998 (1995)
Surrogates for Chiral Aminomalondialdehyde. Synthesis of N-(9-Phenylfluoren-9-yl) serinal and N-(9-Phenylfluoren-9-yl) vinylglycinal.
Lubell WD and Rapoport H.
The Journal of Organic Chemistry, 54(16), 3824-3831 (1989)
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