59737-33-6 Usage
General Description
3-Morpholin-4-yl-propionic acid hydrazide is a chemical compound with the molecular formula C8H16N4O2. Also known as MPHPH, it is a hydrazide derivative with potential anti-tuberculosis activity. 3-MORPHOLIN-4-YL-PROPIONIC ACID HYDRAZIDE has been studied for its potential use in the treatment of tuberculosis, as it has been shown to inhibit the growth of Mycobacterium tuberculosis, the bacteria responsible for the disease. While its exact mechanism of action is not fully understood, it is believed to disrupt the bacterial cell wall synthesis, leading to its antimicrobial effects. 3-MORPHOLIN-4-YL-PROPIONIC ACID HYDRAZIDE is primarily used in research settings to further understand its potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 59737-33-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,3 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59737-33:
(7*5)+(6*9)+(5*7)+(4*3)+(3*7)+(2*3)+(1*3)=166
166 % 10 = 6
So 59737-33-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H15N3O2/c8-9-7(11)1-2-10-3-5-12-6-4-10/h1-6,8H2,(H,9,11)
59737-33-6Relevant articles and documents
An improved procedure for the synthesis of 2-morpholinoethanamine
Yao, Ri-Sheng,Wu, Sheng-Hua,Jiang, Lai-En,Deng, Sheng-Song,Yu, San-Xi
experimental part, p. 523 - 528 (2011/11/30)
2-Morpholinoethanamine is prepared rapidly mainly in aqueous conditions from inexpensive and commercially accessible starting materials. The process development of an effective synthetic route by utilizing morpholine as the starting material via Michael addition, hydrazinolysis, and Curtius rearrangements was undertaken. The optimal conditions were selected in the experiments. The total yield was 81.8% and it was a convenient process. Springer Science+Business Media B.V. 2010.
Derivatives of vicinal trimethoxybenzene. 2. Amide and hydrazide of trimethylgallic acid.
SCHLAGER
, p. 217 - 226 (2007/10/05)
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