712-33-4 Usage
Description
N-3-chloro-4-nitrophenylacetamide is a chemical compound with the molecular formula C8H7ClN2O3. It is an acetamide derivative featuring a chloro-nitro substituted phenyl group. N-3-chloro-4-nitrophenylacetamide is utilized in organic synthesis and pharmaceutical research, and has been investigated for its potential biological activities and pharmacological properties.
Uses
Used in Organic Synthesis:
N-3-chloro-4-nitrophenylacetamide is used as an intermediate in organic synthesis for the production of various organic compounds. Its unique chloro-nitro substituted phenyl group allows for versatile chemical reactions, making it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, N-3-chloro-4-nitrophenylacetamide is used as a starting material or a precursor in the development of new pharmaceuticals. Its potential biological activities and pharmacological properties make it a promising candidate for drug discovery and design.
Used in the Production of Pharmaceuticals:
N-3-chloro-4-nitrophenylacetamide may have applications in the production of various pharmaceuticals. Its unique structure and properties can be leveraged to create new drugs with specific therapeutic effects.
Used in Agrochemicals:
This chemical compound may also find use in the development of agrochemicals, such as pesticides and herbicides. Its potential biological activities could be harnessed to create effective and targeted agrochemicals for agricultural applications.
Safety Considerations:
It is important for researchers and chemists to handle N-3-chloro-4-nitrophenylacetamide with care, as it may pose health and environmental risks. Proper safety measures should be taken to minimize exposure and ensure the safe handling and disposal of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 712-33-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 712-33:
(5*7)+(4*1)+(3*2)+(2*3)+(1*3)=54
54 % 10 = 4
So 712-33-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClN2O3/c1-5(12)10-6-2-3-8(11(13)14)7(9)4-6/h2-4H,1H3,(H,10,12)
712-33-4Relevant articles and documents
Transition-metal-free mono- or dinitration of protected anilines
Dai, Enrui,Dong, Ying,Dong, Yongrui,Kong, Rui,Liang, Deqiang,Liu, Guangzhang,Ma, Yinhai,Wu, Qiong
, (2020/04/27)
An amide-assisted arene nitration is presented, and both mono- and dinitration of protected anilines could be effected by using NaNO2 and NaNO3 as the mono- and bisnitrating agents, respectively. This divergent synthesis is transition-metal- and acid-free, and features a broad substrate scope, low cost, and ortho–para selectivity.
Synthesis of mono-substituted derivatives of 6-aminoquinoline
Lan, Tian,Yuan, Xian Xia,Yu, Jiang Hong,Jia, Chao,Wang, Yu Shi,Zhang, Hui Juan,Ma, Zi Feng,Ye, Wei Dong
experimental part, p. 253 - 255 (2012/01/04)
Several 6-aminoquinoline derivatives, which could be used in drug design, have been synthesized. The reaction conditions were comparatively studied, and the p-chloroaniline was used as optimum oxidant in Skraup-Doebner-Von Miller reaction. The nitro group was reduced effectively by SnCl2 with no halo-removed occurred.
Spectral tuning of azobenzene photoswitches for biological applications
Sadovski, Oleg,Beharry, Andrew A.,Zhang, Fuzhong,Woolley, G. Andrew
scheme or table, p. 1484 - 1486 (2009/07/25)
Longer switching wavelengths and good photochemical yields and stabilities of the cis isomers in reducing aqueous environments are achieved by introducing 2,2 -aminoalkyl substituents into 4,4 - diamido-substituted azobenzenes. The products are thus suita
