368873
9-Bromo-9-phenylfluorene
97%
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About This Item
Empirical Formula (Hill Notation):
C19H13Br
CAS Number:
Molecular Weight:
321.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
mp
99-101 °C (lit.)
functional group
bromo
phenyl
SMILES string
BrC2(c1ccccc1)c3ccccc3-c4ccccc24
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
InChI key
HYQXNCDBSALQLB-UHFFFAOYSA-N
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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)
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)
Configurational stability of N-protected. alpha.-amino aldehydes.
Lubell WD and Rapoport H.
Journal of the American Chemical Society, 109(1), 236-239 (1987)
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)
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