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C19H27NO3 is a chemical compound with the molecular formula consisting of 19 carbon atoms, 27 hydrogen atoms, 1 nitrogen atom, and 3 oxygen atoms. C19H27NO3 belongs to the class of organic compounds, specifically a derivative of a phenol, and is known as a tricyclic phenol. It is a white crystalline solid with a molecular weight of approximately 315.43 g/mol. The compound is characterized by its unique structure, which includes a tricyclic ring system with a hydroxyl group and a nitro group attached to the aromatic ring. It is used in various applications, such as in the synthesis of pharmaceuticals and other organic compounds. Due to its specific functional groups, C19H27NO3 can participate in a range of chemical reactions, including substitution, addition, and elimination reactions, making it a versatile building block in organic chemistry.

7121-51-9

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7121-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7121-51-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,2 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7121-51:
(6*7)+(5*1)+(4*2)+(3*1)+(2*5)+(1*1)=69
69 % 10 = 9
So 7121-51-9 is a valid CAS Registry Number.

7121-51-9Downstream Products

7121-51-9Relevant academic research and scientific papers

Identification of mepenzolate derivatives with long-acting bronchodilatory activity

Tanaka, Ken-Ichiro,Yamakawa, Naoki,Yamashita, Yasunobu,Asano, Teita,Kanda, Yuki,Takafuji, Ayaka,Kawahara, Masahiro,Takenaga, Mitsuko,Fukunishi, Yoshifumi,Mizushima, Tohru

, (2018)

The standard treatment for chronic obstructive pulmonary disease is a combination of anti-inflammatory drugs and bronchodilators. We recently found that mepenzolate bromide (MP), an antagonist for human muscarinic M3 receptor (hM3R), has both anti-inflammatory and short-acting bronchodilatory activities. To obtain MP derivatives with longer-lasting bronchodilatory activity, we synthesized hybrid compounds based on MP and two other muscarinic antagonists with long-acting bronchodilatory activity glycopyrronium bromide (GC) and aclidinium bromide (AD). Of these three synthesized hybrid compounds (MP-GC, GC-MP, MP-AD) and MP, MP-AD showed the highest affinity for hM3R and had the longest lasting bronchodilatory activity, which was equivalent to that of GC and AD. Both MP-GC and MP-AD exhibited an anti-inflammatory effect equivalent to that of MP, whereas, in line with GC and AD, GC-MP did not show this effect. We also confirmed that administration of MP-AD suppressed elastase-induced pulmonary emphysema in a mouse model. These findings provide important information about the structure-activity relationship of MP for both bronchodilatory and anti-inflammatory activities.

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