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Acetyl-N-Propylaniline, also known as N-(2-Propynyl)aniline or 2-Propynylphenylamine, is an organic compound with the chemical formula C9H11N. It is a colorless to pale yellow liquid with a characteristic amine-like odor. ACETYL-N-PROPYLANILINE is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. It is also employed in the production of rubber chemicals and as a curing agent for epoxy resins. Acetyl-N-Propylaniline is known for its reactivity and can undergo various chemical reactions, such as substitution, addition, and condensation, making it a versatile building block in organic synthesis.

2437-98-1

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2437-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2437-98-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2437-98:
(6*2)+(5*4)+(4*3)+(3*7)+(2*9)+(1*8)=91
91 % 10 = 1
So 2437-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO/c1-3-9-12(10(2)13)11-7-5-4-6-8-11/h4-8H,3,9H2,1-2H3

2437-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenyl-N-propylacetamide

1.2 Other means of identification

Product number -
Other names Essigsaeure-propylanilid

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:2437-98-1 SDS

2437-98-1Downstream Products

2437-98-1Relevant academic research and scientific papers

Ruthenium catalysed reduction of alkenes using sodium borohydride

Adair, Gareth R.A.,Kapoor, Kamal K.,Scolan, Alexandre L.B.,Williams, Jonathan M.J.

, p. 8943 - 8944 (2007/10/03)

The reduction of alkenes has been achieved using NaBH4 as the reducing agent using 0.5-1.0 mol % Ru(PPh3)4H2 in the presence of water.

EFFECT OF THE STRUCTURE OF THE AMINE ON THE RATE OF BASE-CATALYZED ACYLATION OF ALKYL AROMATIC AMINES BY BENZOYL CHLORIDE AND 2,4-DINITROPHENYL ACETATE

Oleinik, N. M.,Sadovskii, Yu. S.,Litvinenko, L. M.,Radchenko, N. D.,Korzhilova, L. I.

, p. 1144 - 1152 (2007/10/02)

The kinetics of the noncatalytic and base-catalyzed aminolysis of benzoyl chloride (with pyridine as catalyst) and 2,4-dinitrophenyl acetate (with pyridine, ε-caprolactam and pyridine N-oxide as catalysts) by alkyl aromatic amines PhNHR were studied in benzene at 25 deg C.The obtained rate constants are described satisfactorily by the modified Taft equation, which takes account of the steric and inductive effects of the structure of the amine.The results are discussed in terms of base and nucleophilic mechanisms of catalysis.

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