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104869-86-5

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104869-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104869-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,6 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104869-86:
(8*1)+(7*0)+(6*4)+(5*8)+(4*6)+(3*9)+(2*8)+(1*6)=145
145 % 10 = 5
So 104869-86-5 is a valid CAS Registry Number.

104869-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-nitrophenyl)pentan-3-one

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:104869-86-5 SDS

104869-86-5Downstream Products

104869-86-5Relevant articles and documents

Visible-light-mediated α-arylation of enol acetates using aryl diazonium salts

Hering, Thea,Hari, Durga Prasad,Koenig, Burkhard

, p. 10347 - 10352 (2013/01/15)

Visible light mediates efficiently the α-arylation of enol acetates by aryl diazonium salts under mild conditions using [Ru(bpy)3]Cl 2 as a photoredox catalyst. The broad scope of the reaction toward various diazonium salts and enol acetates was explored. The application of this reaction in the concise synthesis of 2-substituted indoles was demonstrated

A NOVEL NUCLEOPHILIC SUBSTITUTION OF THE FORMYL GROUP IN p-NITROBENZALDEHYDE WITH SOME CARBANIONS

Iwasaki, Genji,Saeki, Seitaro,Hamana, Masatomo

, p. 173 - 176 (2007/10/02)

p-Nitrobenzaldehyde reacts with some active methylene compounds in the presence of a strong base at low temperatures to give p-substituted nitrobenzenes by the two-step course involving the initial formation of the aldol adducts and the subsequent displacement of the carbinol moieties with excess carbanions.

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