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2-amino-5-chloro-N-cyclopropylbenzamide is a chemical compound with the molecular formula C10H11ClN2O. It is a derivative of benzamide, featuring a cyclopropyl group attached to the nitrogen atom, a chlorine atom at the 5th position, and an amino group at the 2nd position on the benzene ring. 2-amino-5-chloro-N-cyclopropylbenzamide is known for its potential applications in pharmaceutical research, particularly as a building block for the synthesis of various drugs. It is also recognized for its role in the development of agrochemicals, where it may be used as a precursor to create compounds with pesticidal properties. The specific applications and effects of 2-amino-5-chloro-N-cyclopropylbenzamide are subject to ongoing scientific investigation and must be evaluated within the context of its chemical properties and potential interactions.

5004-87-5

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5004-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5004-87-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5004-87:
(6*5)+(5*0)+(4*0)+(3*4)+(2*8)+(1*7)=65
65 % 10 = 5
So 5004-87-5 is a valid CAS Registry Number.

5004-87-5Relevant academic research and scientific papers

Synthesis and biological evaluation of novel N-pyridylpyrazolecarboxamides containing benzothiazole

Mao, Ming-Zhen,Wang, Hai-Yang,Wang, Wei,Ning, Bin-Ke,Li, Yu-Xin,Xiong, Li-Xia,Li, Zheng-Ming

, p. 42 - 46 (2016/12/24)

A series of novel N-pyridylpyrazolecarboxamides containing benzothiazolewere designed and synthesized. The target compounds were identified by 1H NMR,13C-NMR, IR, high-resolution mass spectrum (HRMS) and elemental analysis. The bioactivities of the newcom

Synthesis, Crystal Structure, and Biological Activity of Novel Anthranilic Diamide Insecticide Containing Propargyl Ether Group

Huang, Zhiqiang,Tong, Jun,Zhou, Sha,Xiong, Lixia,Wang, Hongxue,Zhao, Yu

, p. 1036 - 1045 (2016/07/28)

In search of environmentally benign insecticides with high activity, low toxicity, and low residue, a series of novel anthranilic diamide containing propargyl ether were designed and synthesized. All compounds were characterized by1H NMR spectroscopy, high-resolution mass spectrometry, or elemental analysis. The single crystal structure of 18g was determined by X-ray diffraction. The insecticidal activities against Lepidoptera pests of the new compounds were evaluated. Their insecticidal activities against oriental armyworm (Mythimna separata) and diamondback moth (Plutella xylostella) indicated that most of the compounds showed moderate to high activities at the tested concentration.

Synthesis, crystal structure and biological activity of a novel anthranilic diamide insecticide containing allyl ether

Zhao, Yu,Xiong, Li-Xia,Xu, Li-Ping,Wang, Hongxue,Xu, Han,Li, Hua-Bin,Tong, Jun,Li, Zheng-Ming

, p. 3071 - 3088 (2013/09/23)

In search of environmentally benign insecticides with high activity, low toxicity and low residue, a series of novel anthranilic diamides containing allyl ether were designed and synthesized. All the compounds were characterized by 1H NMR spectroscopy, HRMS or elemental analysis. The single crystal structure of 18e was determined by X-ray diffraction. The insecticidal activities of the new compounds were evaluated. The results showed that some compounds exhibited excellent insecticidal activities against Lepidoptera pests. Among this series compounds, 18l showed 100 % larvicidal activity against Mythimna separate Walker and Plutella xylostella Linnaeus at the test concentration.

Design, synthesis and biological activities of novel anthranilic diamide insecticide containing trifluoroethyl ether

Zhao, Yu,Li, Yongqiang,Xiong, Lixia,Wang, Hongxue,Li, Zhengming

, p. 1748 - 1758 (2012/11/13)

Two series of novel anthranilic diamide insecticide containing trifluoroethyl ether were designed and synthesized, and their structures were characterized by 1H NMR spectroscopy, elemental analysis and single crystal X-ray diffraction analysis. The insecticidal activities of the new compounds were evaluated. The results of bioassays indicated that some of these title compounds exhibited excellent insecticidal activities. The insecticidal activities of compounds 19a, 19b, 19d, 19g, 19k and 19m against oriental armyworm at 2.5 mg·kg-1 were 100%. The larvicidal activities of 19a, 19b, 19c, 19d, 19e, 19g and 19n against diamond-back moth were 100% at 0.1 mg·kg-1. Surprisingly, most of them still exhibited perfect insecticidal activity against diamond-back moth when the concentration was reduced to 0.05 mg·kg-1, which was higher than the commercialized Chlorantraniliprole.

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