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Benzenamine, 4-fluoro-N-sulfinyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52326-08-6

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52326-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52326-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,2 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52326-08:
(7*5)+(6*2)+(5*3)+(4*2)+(3*6)+(2*0)+(1*8)=96
96 % 10 = 6
So 52326-08-6 is a valid CAS Registry Number.

52326-08-6SDS

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 N-sulfinyl-4-fluoroaniline

1.2 Other means of identification

Product number -
Other names 4-fluoro-N-sulfinylaniline

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:52326-08-6 SDS

52326-08-6Upstream product

52326-08-6Relevant articles and documents

Synthesis of benzothiazine sulfonamides via heteroatomic Diels-Alder reaction of para-fluoro-N-sulfinylaniline with bicyclo[2.2.1]heptenes

Veremeichik,Shurpik,Lodochnikova,Plemenkov

, p. 296 - 299 (2016)

Reaction of 4-fluoro-N-sulfinylaniline with norbornene and norbornadiene has afforded the Diels-Alder adducts of benzothiazine structure that have been oxidized into the corresponding benzothiazine sulfonamides. Structure of the obtained compounds and ste

Synthesis, characterization and vibrational properties of p-fluorosulfinylaniline

Jerez, Ana L. Pez,Antognini, Andrea Flores,Cutin, Edgardo H.,Robles, Norma L.

, p. 300 - 305 (2015)

The reaction of p-fluoroaniline and SOCl2 rendered p-fluorosulfinylaniline in good yield. The obtained dark yellowish liquid compound was characterized by NMR, UV-visible, FT-IR and Raman spectroscopies. The observed features were consistent wi

Synthesis of six-membered cyclic sulfonimidamides

Sen, Indira,Kloer, Daniel,Hall, Roger,Pal, Sitaram

, p. 3018 - 3028 (2013/11/06)

A general synthetic route to six-membered cyclic N-aryl- and N-alkyl-substituted sulfonimidamides via an intramolecular ring closure of suitably functionalised acyclic sulfonimidamides is described. The structure of this new ring system was confirmed by v

N-heterocyclic carbene catalysis: Enantioselective formal [2+2] cycloaddition of ketenes and N-sulfinylanilines

Jian, Teng-Yue,He, Lin,Tang, Cen,Ye, Song

supporting information; body text, p. 9104 - 9107 (2011/10/13)

Sultam of swing: Both enantiomers of 1,2-thiazetidin-3-one oxides were obtained in very good yields with excellent enantioselectivities when using N-heterocyclic carbene catalysts (see scheme; M.S.=molecular sieves, TBS=tert-butyldimethylsilyl). The products were easily converted into 3-oxo-β-sultams, α-mercapto amides, and β-mercapto amines through oxidation or reduction. Copyright

Substituted N-aryl alk-1-enesulfinamides: Preparation, properties and conversion into the corresponding indole compounds [1]

Baudin, Jean-Bernard,Commenil, Marie-Gabrielle,Julia, Sylvestre A.,Lorne, Robert,Mauclaire, Laurent

, p. 329 - 350 (2007/10/03)

Reaction of vinylic organometallic derivatives with N-sulfinyl arenamines 2 affords the title sulfinamides 3. On heating their solutions in selected solvents to 80-124 °C, these sulfinamides are converted into the corresponding indoles 6, probably via a [3.3]-sigmatropic rearrangement to intermediates VIII which undergo an intramolecular carbophilic reaction of the nitrogen atom with the neighboring sulfine group, followed by elimination of HSOH. The triethyloxonium tetrafluoroborate- or boron trifluoride etherate catalyzed conversion 3 → 6 can be carried out at a much lower temperature. Elsevier,.

Reactions of N-sulfinylfluoroalkanesulfonyl amines with nucleophiles containing reactive hydrogen

Li, Ai-Wen,Xu, Bin,Wang, Chao-Xian,Zhu, Shi-Zheng

, p. 85 - 88 (2007/10/02)

The reactions of N-sulfinylfluoroalkanesulfonyl amines, RfSO2NSO (1), with malonate or dialkyl phosphite gave 1:1 adducts RfSO2NHS(O)Nu , and with alcohols or phenols formed RfSO2NH2 and the sulfites O=S(OR)2 by double addition .Trans-sulfinylation occurred during the reaction of 1 with anilines (C6H5NH2, 4-FC6H4NH2 and C6F5NH2).

Umsetzungen von Metall- und Metalloidverbindungen mit mehrfunktionellen Molekuelen, XXVI Reaktionen von N-Sulfinylverbindungen mit Thioboranen

Meller, Anton,Maringgele, Walter,Fetzer, Hartmut

, p. 1950 - 1961 (2007/10/02)

The reaction of N-sulfinylamines with (methylthio)organylboranes proceeds quantitatively according to R-N=S=O + 3 R'2BSCH3 -> RN(BR'2)-SSCH3 + CH3SSCH3 + 2O by insertion of the N=S double bond into the B-S sequence and a complex redox-reaction.Th

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