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7-phenyl-7H-benzo[c]fluorene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32377-10-9

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32377-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32377-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,7 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32377-10:
(7*3)+(6*2)+(5*3)+(4*7)+(3*7)+(2*1)+(1*0)=99
99 % 10 = 9
So 32377-10-9 is a valid CAS Registry Number.

32377-10-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-phenyl-7H-benzo[c]fluorene

1.2 Other means of identification

Product number -
Other names 7-PHENYL-7H-BENZO(C)FLUORENE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:32377-10-9 SDS

32377-10-9Downstream Products

32377-10-9Relevant academic research and scientific papers

Heterobimetallic Pd-Sn catalysis: A Suzuki, tandem ring-closing sequence toward indeno[2,1-b]thiophenes and indeno[2,1-b]indoles

Das, Debjit,Pratihar, Sanjay,Roy, Sujit

, p. 4870 - 4873,4 (2020/09/16)

Indeno[2,1-b]thiophene and indeno[1,2-b]indole motifs have been obtained in moderate to good yields from easily available substituted boronic acids, 2-bromo aryl/vinyl aldehydes, and nucleophiles such as arenes/heteroarenes and others using a catalytic co

Highly efficient synthesis of polysubstituted fluorene via iron-catalyzed intramolecular Friedel-Crafts alkylation of biaryl alcohols

Sarkar, Soumen,Maiti, Sukhendu,Bera, Krishnendu,Jalal, Swapnadeep,Jana, Umasish

, p. 5544 - 5547 (2012/11/07)

An efficient and mild Fe(III)-catalyzed intramolecular Friedel-Crafts alkylation of biaryl methanol derivatives has been developed to achieve the substituted fluorene derivatives. The present reaction provides an excellent alternative to published methods

PHOTOCHEMICAL REACTIONS OF TRIARYLMETHYL PEROXIDES (II) α- AND β-NAPHTHYLDIPHENYLMETHYL PEROXIDE

Neckers, D. C.,Linden, Shwn-Mei,Taliano, Ross J.,Williams, B. Lee,Zakrzewski, Andrei

, p. 3029 - 3032 (2007/10/02)

The photochemical decomposition of the title compounds and isotopically labeled analogs have been compared to the thermal rections.Rapid radical 1,2-migration and reversible elimination of oxygen from the starting peroxides are indicated.

Carbon Acidity. 72. Ion Pair Acidities of Phenyl Alkyl Ketones. Aggregation Effects in Ion Pair Acidities

Kaufman, Michael J.,Streitwieser, Andrew

, p. 6092 - 6097 (2007/10/02)

Equilibrium cesium ion pair acidities of acetophenone, propiophenone, isobutyrophenone, and o-methoxyacetophenone and the lithium ion pair acidity of o-methoxyacetophenone in tetrahydrofuran have been determined by an indicator method.For all of these compounds, the observed pKa values decrease as the equilibrium enolate concentration is increased.It is proposed that this concentration dependence is a consequence of the aggregation of the enolates, and a method is described whereby average aggregation numbers can be determined from the acidity data.The results indicate that the extent of aggregation of enolate ions is influenced by both electronic and steric factors.In addition, internal solvation is found to be important for the lithium, but not the cesium enolate of o-methoxyacetophenone.

GENERATION AND THERMAL BOND RELOCATION OF A STERICALLY CONGESTED CYCLOTETRAENYL ANION

Anastassiou, A. G.,Kasmai, H. S.,Hasan, M.

, p. 1695 - 1698 (2007/10/02)

The sterically strained anion 4 was found to be thermally labile to subzero workup, readily undergoing temperature-dependent electrocyclization to a variety of tetracyclic frames.

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