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N-butyl-N-phenylbutanamide is a chemical compound with the molecular formula C16H23NO. It is an amide derivative, characterized by the presence of a carbonyl group (C=O) bonded to a nitrogen atom (N). The compound consists of a butyl group (C4H9) attached to the nitrogen atom, a phenyl group (C6H5) attached to the carbonyl carbon, and a butanamide group (C4H7O). N-butyl-N-phenylbutanamide is a colorless to pale yellow liquid with a mild, aromatic odor. It is used in various applications, including as a solvent, a chemical intermediate, and in the synthesis of pharmaceuticals and agrochemicals. Due to its specific structure and properties, it may exhibit unique reactivity and solubility characteristics, making it a valuable component in the development of new chemical products.

6289-67-4

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6289-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6289-67-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6289-67:
(6*6)+(5*2)+(4*8)+(3*9)+(2*6)+(1*7)=124
124 % 10 = 4
So 6289-67-4 is a valid CAS Registry Number.

6289-67-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butyl-N-phenylbutyramide

1.2 Other means of identification

Product number -
Other names N-Butyl-butyranilid

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:6289-67-4 SDS

6289-67-4Downstream Products

6289-67-4Relevant academic research and scientific papers

Iron-catalyzed oxidative amidation of tertiary amines with aldehydes

Li, Yuanming,Jia, Fan,Li, Zhiping

supporting information, p. 82 - 86 (2013/03/13)

Unconventional couple: A new oxidative coupling protocol for amide bond formation has been developed (see scheme). The method provides an efficient and practical route for the synthesis of tertiary amides from readily available tertiary amines and aldehydes in the presence of a simple FeCl2 catalyst. Mechanistic studies indicated that a peroxide and an iminium ion act as the reactive intermediates in this oxidative amidation.

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