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Benzenamine, 4-chloro-N-[(pentafluorophenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90283-13-9

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90283-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90283-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,8 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90283-13:
(7*9)+(6*0)+(5*2)+(4*8)+(3*3)+(2*1)+(1*3)=119
119 % 10 = 9
So 90283-13-9 is a valid CAS Registry Number.

90283-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-chlorophenyl)-1-(2,3,4,5,6-pentafluorophenyl)methanimine

1.2 Other means of identification

Product number -
Other names Benzenamine,4-chloro-N-[(pentafluorophenyl)methylene]

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:90283-13-9 SDS

90283-13-9Relevant academic research and scientific papers

Perfluorophenyl phosphonate analogues of aromatic amino acids: Synthesis, X-ray and DFT studies

Paw?owska, Agata,Volle, Jean-No?l,Virieux, David,Pirat, Jean-Luc,Janiak, Agnieszka,Nowicki, Mateusz,Hoffmann, Marcin,Pluskota-Karwatka, Donata

, p. 975 - 986 (2018/01/27)

Novel perfluorophenyl phosphonate analogues of phenylglycine and homophenylalanine were prepared in good to excellent yields, and subjected to solid state characterization by single-crystal X-ray diffraction analysis, and to investigations with the use of

Multicomponent assembly of 4-aza-podophyllotoxins: A fast entry to highly selective and potent anti-leukemic agents

Jeedimalla, Nagalakshmi,Flint, Madison,Smith, Lyndsay,Haces, Alberto,Minond, Dmitriy,Roche, Stéphane P.

supporting information, p. 167 - 179 (2015/11/17)

The aim of this study was the synthesis and lead structure selection of a best anti-leukemic agent from a library of aza-podophyllotoxin analogues (APTs). To this end, we report a scalable, modified multicomponent reaction using a "sacrificial" aniline pa

One-pot synthesis of 1,2,3,4-tetrafluoroacridines from pentafluorobenzaldehyde

Adamson, Adrian J.,Banks, R. Eric,Fields, Roy,Tipping, Anthony E.

, p. 530 - 555 (2007/10/03)

Treatment of pentafluorobenzaldehyde with a two-molar equivalence of aniline in o-dichlorobenzene at ca. 180 yields a complex mixture of products from which 1,2,3,4-tetrafluoroacridine (1a) and its 3-anilino derivative (7a) can be isolated in at least 48

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