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3-Nitrophenyl dimethylcarbamate is an organic compound with the chemical formula C9H10N2O5. It is a derivative of phenol, where a nitro group (-NO2) is attached to the phenyl ring at the 3rd position, and a dimethylcarbamate group (-CO(N(CH3)2)) is attached to the same phenyl ring. 3-nitrophenyl dimethylcarbamate is known for its potential use as an intermediate in the synthesis of various agrochemicals and pharmaceuticals. It is also recognized for its herbicidal properties, particularly in the control of certain types of weeds. The compound is characterized by its yellow crystalline appearance and is typically handled with care due to its potential toxicity and reactivity.

7304-99-6

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7304-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7304-99-6 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 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7304-99:
(6*7)+(5*3)+(4*0)+(3*4)+(2*9)+(1*9)=96
96 % 10 = 6
So 7304-99-6 is a valid CAS Registry Number.

7304-99-6SDS

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 (3-nitrophenyl) N,N-dimethylcarbamate

1.2 Other means of identification

Product number -
Other names 3-nitrophenyl dimethylcarbamate

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:7304-99-6 SDS

7304-99-6Relevant academic research and scientific papers

An efficient method for the protection of aromatic amines with benzostabase and its utility in anionic aromatic transformations

Lu, Erhu,Yadav, Arun,Weaver, Donald F.,Reed, Mark A.

supporting information, p. 2259 - 2262 (2013/11/06)

Herein we describe an efficient and generally applicable method of protecting a diverse series of aromatic amines with the 'benzostabase' group. We also demonstrate its efficient use in aromatic anionic chemistry including its utility in the anionic ortho

Pd(II)-catalyzed C-H activation/aryl-aryl coupling of phenol esters

Xiao, Bin,Fu, Yao,Xu, Jun,Gong, Tian-Jun,Dai, Jian-Jun,Yi, Jun,Liu, Lei

supporting information; experimental part, p. 468 - 469 (2010/03/25)

(Chemical Equation Presented) Although nitrogen-containing group-directed cyclopalladation reactions have been well-known, Pd(II) insertion into C-H bonds promoted by coordination of an oxygen-only group to the palladium remains rather rare. In the present study, the first cyclopalladation complex formed from a simple phenol ester was characterized by X-ray crystallography. A promising protocol for the ortho C-H activation/aryl-aryl coupling of phenol esters that was not sensitive to moisture or air was then established. The utility of the reaction was demonstrated for the synthesis of useful phenol derivatives. Copyright

Novel class of LIM-kinase 2 inhibitors for the treatment of ocular hypertension and associated glaucoma

Harrison, Bryce A.,Whitlock, N. Andrew,Voronkov, Michael V.,Almstead, Zheng Y.,Gu, Kun-Jian,Mabon, Ross,Gardyan, Michael,Hamman, Brian D.,Allen, Jason,Gopinathan, Suma,McKnight, Beth,Crist, Mike,Zhang, Yulian,Liu, Ying,Courtney, Lawrence F.,Key, Billie,Zhou, Julia,Patel, Nita,Yates, Phil W.,Liu, Qingyun,Wilson, Alan G. E.,Kimball, S. David,Crosson, Craig E.,Rice, Dennis S.,Rawlins, David B.

supporting information; experimental part, p. 6515 - 6518 (2010/03/31)

The discovery of a pyrrolopyrimidine class of LIM-kinase 2 (LIMK2) inhibitors is reported. These LIMK2 inhibitors show good potency in enzymatic and cellular assays and good selectivity against ROCK. After topical dosing to the eye in a steroid induced mouse model of ocular hypertension, the compounds reduce intraocular pressure to baseline levels. The compounds also increase outflow facility in a pig eye perfusion assay. These results suggest LIMK2 may be an effective target for treating ocular hypertension and associated glaucoma.

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