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N-[4-(dimethylamino)phenyl]-N-methylformamide is an organic compound with the chemical formula C11H16N2O. It is a derivative of formamide, featuring a phenyl ring with a dimethylamino group at the para position and a methylformamide group attached to the nitrogen atom. N-[4-(dimethylamino)phenyl]-N-methylformamide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is a colorless to pale yellow solid and is soluble in common organic solvents. The compound is also referred to as 4-(dimethylamino)phenyl-N-methylformamide or N-methyl-N-[4-(dimethylamino)phenyl]formamide. It is important to handle this chemical with care due to its potential toxicity and reactivity, and it is typically used in a controlled laboratory setting for the synthesis of target compounds.

2739-06-2

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2739-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2739-06-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2739-06:
(6*2)+(5*7)+(4*3)+(3*9)+(2*0)+(1*6)=92
92 % 10 = 2
So 2739-06-2 is a valid CAS Registry Number.

2739-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-(dimethylamino)phenyl]-N-methylformamide

1.2 Other means of identification

Product number -
Other names N,N'-Trimethyl-N'-formyl-p-phenylendiamin

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:2739-06-2 SDS

2739-06-2Relevant academic research and scientific papers

Ligand-Enabled Ni-Al Bimetallic Catalysis for Nonchelated Dual C-H Annulation of Arylformamides and Alkynes

Luan, Yu-Xin,Wang, Yin-Xia,Ye, Mengchun,Zhang, Feng-Ping

supporting information, (2020/03/19)

A bifunctional secondary phosphine oxide (SPO) ligand-controlled method was developed for Ni-Al-catalyzed nonchelated dual C-H annulation of arylformamides with alkynes, providing a series of substituted amide-containing heterocycles in ≤97% yield. The SPO-bound bimetallic catalysis proved to be critical to the reaction efficiency.

Direct condensation of functionalized sp3 carbons with formanilides for enamine synthesis using an in situ generated HMDS amide catalyst

Taneda, Hiroshi,Inamoto, Kiyofumi,Kondo, Yoshinori

supporting information, p. 6523 - 6525 (2014/06/09)

The efficient synthesis of functionalized enamines including β-enaminoesters was effectively accomplished by the direct condensation of functionalized sp3 carbanions such as acetates with formamides using in situ generated HMDS base from catalytic cesium fluoride and stoichiometric tristrimethylsilylamine. This journal is the Partner Organisations 2014.

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