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(4-nitro-phenyl)-acetyl azide is an organic compound with the chemical formula C8H6N4O3. It is a derivative of phenylacetic acid, where the carboxylic acid group is replaced by an azide group, and the phenyl ring is substituted with a nitro group at the para position. (4-nitro-phenyl)-acetyl azide is known for its reactivity and is often used in chemical synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. It is also utilized in the synthesis of dyes and other specialty chemicals. Due to the presence of the azide group, which is highly reactive and can undergo a variety of chemical transformations, (4-nitro-phenyl)-acetyl azide is a valuable intermediate in organic chemistry. However, it should be handled with care due to the potential hazards associated with azide compounds, such as their sensitivity to heat and shock.

6144-82-7

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6144-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6144-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,4 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6144-82:
(6*6)+(5*1)+(4*4)+(3*4)+(2*8)+(1*2)=87
87 % 10 = 7
So 6144-82-7 is a valid CAS Registry Number.

6144-82-7Relevant academic research and scientific papers

2-(iminomethyl) amino-phenyl derivatives, preparation, application as medicines and pharmaceutical compositions containing same

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Page column 33, (2008/06/13)

A compound of the formula wherein the substituents are defined as in the specification and their pharmaceutically acceptable salts having NOS and ROS activity.

Orally Active β-Lactam Inhibitors of Leukocyte Elastase-1. Activity of 3,3-Diethyl-2-azetidinones

Shah, Shrenik K.,Dorn, Conrad P.,Finke, Paul E.,Hale, Jeffrey J.,Hagmann, William K.,et al.

, p. 3745 - 3754 (2007/10/02)

A thorough analysis of the mechanism of inhibition of human leukocyte elastase (HLE) by a monocyclic β-lactam and the mechanism of β-lactam hydrolysis led to the preparation of potent and highly stable inhibitors of HLE.This work led to the identification of 4--3,3-diethyl-1-carbonyl>-2-azetidinone (2) as the first orally active inhibitor of human leukocyte elastase (HLE).Analogs of 2 with different substituents on the urea N were synthesized and evaluated for their activity in vitro against HLE as well as in vivo in a hamster lung hemorrhage model.Compounds with a methyl or a methoxy group in the para position of the benzene ring were very potent in both assays.The results are discussed on the basis of the proposed model for the binding of this class of inhibitors to HLE and a possible mechanism of inhibition is presented.

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