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1-Penten-3-one, 1-hydroxy-4,4-dimethyl-1-(4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105590-53-2

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105590-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105590-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,9 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105590-53:
(8*1)+(7*0)+(6*5)+(5*5)+(4*9)+(3*0)+(2*5)+(1*3)=112
112 % 10 = 2
So 105590-53-2 is a valid CAS Registry Number.

105590-53-2SDS

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 p-Nitro-benzoyl-[pivaloyl]-methan (Enolform), 1-(p-Nitrophenyl)-1-hydroxy-3-oxo-4,4-dimethyl-penten-(1)

1.2 Other means of identification

Product number -
Other names p-Nitro-benzoyl-(pivaloyl)-methan (Enolform), 1-(p-Nitrophenyl)-1-hydroxy-3-oxo-4,4-dimethyl-penten-(1)

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:105590-53-2 SDS

105590-53-2Downstream Products

105590-53-2Relevant academic research and scientific papers

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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