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O-bromophenyl N,N-dimethylcarbamate is an organic compound with the chemical formula C9H10BrNO2. It is a derivative of phenol, where a bromine atom is attached to the ortho position (the second carbon) of the phenyl ring. The molecule also contains a carbamate functional group, which is formed by the reaction of the phenol hydroxyl group with N,N-dimethylamine, resulting in the formation of an ester-like linkage. o-bromophenyl N,N-dimethylcarbamate is characterized by its potential reactivity and may have applications in the synthesis of pharmaceuticals or other organic compounds. It is important to handle such chemicals with care due to their potential toxicity and reactivity.

7305-04-6

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7305-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7305-04-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,0 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7305-04:
(6*7)+(5*3)+(4*0)+(3*5)+(2*0)+(1*4)=76
76 % 10 = 6
So 7305-04-6 is a valid CAS Registry Number.

7305-04-6Relevant academic research and scientific papers

Rhodium-Catalyzed ortho-Bromination of O-Phenyl Carbamates Accelerated by a Secondary Amide-Pendant Cyclopentadienyl Ligand

Tanaka, Jin,Shibata, Yu,Joseph, Anton,Nogami, Juntaro,Terasawa, Jyunichi,Yoshimura, Ryo,Tanaka, Ken

supporting information, p. 5774 - 5779 (2020/05/08)

It has been established that a newly developed cyclopentadienyl rhodium(III) [CpARhIII] complex, bearing an acidic secondary amide moiety on the Cp ring, is able to catalyze the ortho-bromination of O-phenyl carbamates with N-bromosuccinimide (NBS) at room temperature. The presence of the acidic secondary amide moiety on the CpA ligand accelerates the bromination by the hydrogen bond between the acidic NH group of the CpA ligand and the carbonyl group of NBS.

Ligand-assisted copper-catalyzed oxidative cross-coupling of simple phenols with formamides for the synthesis of carbamates

Reddy, Nagireddy Veera,Kumar, Gadde Sathish,Kumar, Pailla Santhosh,Kantam, M. Lakshmi,Reddy, Kallu Rajender

supporting information, p. 2133 - 2138 (2014/11/08)

An oxidative approach for the synthesis of phenyl carbamates has been achieved by ligand-assisted copper-catalyzed cross-dehydrogenative coupling (CDC) of phenols with formamides. The direct coupling of simple phenols with mono- and dialkyl formamides pro

Palladium catalyzed C-H functionalization of O-arylcarbamates: Selective ortho -bromination using NBS

John, Alex,Nicholas, Kenneth M.

, p. 5600 - 5605 (2012/07/30)

A series of cyclometalated palladium complexes derived from O-phenylcarbamates has been synthesized by the reaction of the respective carbamates with Pd(OAc)2 in the presence of acids, CF 3CO2H, CF3SO3/sub

High-yielding, versatile, and practical [Rh(III)Cp*]-catalyzed ortho bromination and iodination of arenes

Schroeder, Nils,Wencel-Delord, Joanna,Glorius, Frank

supporting information; experimental part, p. 8298 - 8301 (2012/06/29)

We report a uniquely high-yielding, general, and practical ortho bromination and iodination reaction of different classes of aromatic compounds. This reaction occurs by Rh(III)-catalyzed C-H bond activation methodology and is therefore the first example of the application of this cationic catalyst for C-Br and C-I bond formation.

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