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75158-95-1

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75158-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75158-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,5 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75158-95:
(7*7)+(6*5)+(5*1)+(4*5)+(3*8)+(2*9)+(1*5)=151
151 % 10 = 1
So 75158-95-1 is a valid CAS Registry Number.

75158-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Nitro-fluorenon-anil

1.2 Other means of identification

Product number -
Other names -

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:75158-95-1 SDS

75158-95-1Relevant articles and documents

An aryl to imidoyl palladium migration process involving intramolecular C-H activation

Zhao, Jian,Yue, Dawei,Campo, Marino A.,Larock, Richard C.

, p. 5288 - 5295 (2008/02/02)

Biologically interesting fluoren-9-one and xanthen-9-one derivatives have been prepared by a novel aryl to imidoyl palladium migration, followed by intramolecular arylation. The fluoren-9-one synthesis appears to involve both a palladium migration mechanism and a C-H activation process proceeding through an unprecedented organopalladium(IV) hydride intermediate. The results from deuterium labeling experiments are consistent with the proposed dual mechanism.

Synthesis of Phosphonic Analogues of Morphactines

Gancarz, R.,Wieczorek, J. S.

, p. 213 - 222 (2007/10/02)

9-Aminofluorenphosphonsaeuren (Morphaktine) entstehen durch Addition von Diethylphosphit an 9-Imino-fluorenderivate.Die primaer erhaltenen Ester werden zu den korrespondierenden Saeuren hydrolysiert, eine Reihe der Aminophosphonsaeuren zerfallen unter den

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