콘텐츠로 건너뛰기
Merck
모든 사진(2)

주요 문서

366641

Sigma-Aldrich

9-Phenyl-9-fluorenol

99%

로그인조직 및 계약 가격 보기


About This Item

실험식(Hill 표기법):
C19H14O
CAS Number:
Molecular Weight:
258.31
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

99%

양식

solid

mp

93-95 °C (lit.)

작용기

hydroxyl
phenyl

SMILES string

OC2(c1ccccc1)c3ccccc3-c4ccccc24

InChI

1S/C19H14O/c20-19(14-8-2-1-3-9-14)17-12-6-4-10-15(17)16-11-5-7-13-18(16)19/h1-13,20H

InChI key

UJPHBDAPVWFPTG-UHFFFAOYSA-N

일반 설명

9-Phenyl-9-fluorenol is a fluorine derivative. It is formed as intermediate during the synthesis of 9-bromo-9-phenylfluorene. Competitive interactions in crystalline 9-phenyl-9-fluorenol has been reported. Spectral properties of 9-phenyl-9-fluorenol have been investigated. 9-Phenyl-9-fluorenol is reported as bichromphoric fluorine derivative and its absorption and emission characteristics have been investigated in non-polar and polar solvents at different temperatures.

애플리케이션

9-Phenyl-9-fluorenol may be used as reagent in the synthesis of trisphosphine alkoxide complexes. It may be useful in the preparation of 2,2′-biphenol monobenzoate and is a convenient source of the 9-phenylfluorenyl cation.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number

적합한 버전을 찾을 수 없으신가요?

특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

이미 열람한 고객

Slide 1 of 2

1 of 2

Competitive interactions in crystalline 9-pyridyl-9-fluorenols: crossover from O-HO to O-HN hydrogen bonding to construct intra-and intermolecular, helical and linear contact modes.
Hosseinzadeh R, et al.
CrystEngComm, 11(7), 1331-1337 (2009)
Journal of the Chemical Society. Perkin Transactions 1, 931-931 (1989)
Pinjing Zhao et al.
Journal of the American Chemical Society, 128(10), 3124-3125 (2006-03-09)
beta-Aryl eliminations from a series of rhodium(I) alkoxides to form rhodium aryl complexes and free ketones are reported. Tertiary phenylmethoxide complexes [Rh(PEt3)n(OCPhRR')] (n = 2, 3) were prepared via alcoholysis of {Rh(PEt3)2[N(SiMe3)2} by the corresponding alcohols HOCPhRR' in the presence
Spectroscopic Study of Solvatochromic Effects in Solution of Amino and Hydroxy Derivatives of Fluorene.
Redzimski T and Heldt JR.
Journal of Fluorescence, 13(5), 393-401 (2003)
9-Bromo-9Phenylfluorene.
Jamison TF, et al.
Organometallic Syntheses, 220-220 (1993)

자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..

고객지원팀으로 연락바랍니다.