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Cyclooctane, 1-fluoro-2-(phenylseleno)-, (1R,2R)-rel- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102998-87-8

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102998-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102998-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,9,9 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 102998-87:
(8*1)+(7*0)+(6*2)+(5*9)+(4*9)+(3*8)+(2*8)+(1*7)=148
148 % 10 = 8
So 102998-87-8 is a valid CAS Registry Number.

102998-87-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-2-phenylselenylcyclooctane

1.2 Other means of identification

Product number -
Other names (1S,2S)-1-Fluoro-2-phenylselanyl-cyclooctane

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:102998-87-8 SDS

102998-87-8Downstream Products

102998-87-8Relevant academic research and scientific papers

Phenylselenofluorination of alkenes and alkynes promoted by difluoroiodotoluene and diphenyldiselenide

Panunzi, Barbara,Picardi, Andrea,Tingoli, Marco

, p. 2339 - 2342 (2007/10/03)

The oxidation of diphenyldiselenide with 4-iodotoluene difluoride (DFIT) in dichloromethane produces in situ an efficient phenylselenofluorinating agent of alkenes and internal alkynes.

Electrochemical Fluoro-Chalcogenation

Uneyama, Kenji,Asai, Hideki,Dan-Oh, Yasufumi,Funatsuki, Hiroshi

, p. 395 - 396 (2007/10/03)

Electrochemical fluoro-chalcogenation (S, Se) of alkenes and alkynes, and recycle use of in situ generated PhSeF for allylic fluorination are discussed.

Phenylthio (and phenylseleno)fluorination of alkenes and alkynes using N-phenylthio (and phenylseleno)phthalimide combined with pyridine*9HF or Et3N*3HF complexes

Saluzzo, Christine,Spina, Anna-Maria La,Picq, Dominique,Alvernhe, Gerard,Anker, Daniel,et al.

, p. 831 - 843 (2007/10/02)

N-Phenylthiophthalimide and N-phenylselenophthalimide combined with pyridine*9HF or Et3N*3HF complexes allow the formal addition of elements of PHSF or PhSeF across the carbon-carbon double or triple bond by a one-pot reaction.Pyridine*9HF, a strongly aci

PHENYLSELENOFLUORATION D'ALCENES ACIDO-SENSIBLES

Saluzzo, Christine,Alvernhe, Gerard,Anker, Daniel,Haufe, Guenter

, p. 663 - 666 (2007/10/02)

β-phenylselenofluorides have been synthesized by reaction of olefins (even acido-sensitive ones) with N-phenylselenophthalimide in the presence of triethylamine tris-hydrofluoride.Owing to the regioselectivity observed, this reaction constitutes a good me

N-PHENYLSELENOPHTHALIMIDE (NPSP) A VALUABLE SELENENYLATING AGENT

Nicolaou, K. C.,Petasis, N. A.,Claremon, D. A.

, p. 4835 - 4842 (2007/10/02)

The phenylseleno group (PhSe) has evolved in recent years as a very useful and versatile functionality.Its facile introduction into organic molecules and its subsequent oxidative or reductive removal, has allowed many important synthetic transformations.D

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