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2-(morpholin-4-ylmethyl)-1H-naphtho[2,3-d]imidazole is a complex organic compound with the molecular formula C16H16N4O. It is characterized by a naphthalene ring fused to an imidazole ring, with a morpholine group attached to the 2-position of the imidazole. 2-(morpholin-4-ylmethyl)-1H-naphtho[2,3-d]imidazole is of interest in medicinal chemistry due to its potential biological activities, such as acting as a histamine H3 receptor antagonist, which can be relevant for the treatment of various central nervous system disorders. The structure of 2-(morpholin-4-ylmethyl)-1H-naphtho[2,3-d]imidazole allows for potential interactions with biological targets, making it a subject of research in drug development.

6000-17-5

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6000-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6000-17-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6000-17:
(6*6)+(5*0)+(4*0)+(3*0)+(2*1)+(1*7)=45
45 % 10 = 5
So 6000-17-5 is a valid CAS Registry Number.

6000-17-5Downstream Products

6000-17-5Relevant academic research and scientific papers

Total synthesis of 3-hydroxy-6-oxaestra-1,3,5(10)-trien-17-one

Cao, Zhisong,Liehr, Joachim G.

, p. 841 - 844 (1996)

The modified steroid estrogen, 3-hydroxy-6-oxaestra-1,3,5(10)-trien-17-one, i.e. 6-oxaestrone 8 has been prepared from 7-methoxychromanone 1 by de novo synthesis of the modified steroid ring system. The 1H and 13C NMR data for the intermediate products 3, 4, 4a, 4b, 4c, 6, 7, and for the final product 8 support the proposed structures. A mechanism for the ring-closure reaction of 3 to intermediate products 4 and 4a is proposed.

Synthesis of 6-oxaestra-1,3,5(10),8,14-pentaenes

Abusalimov,Nikol'skaya,Starova,Selivanov,Shavva

, p. 42 - 47 (2007/10/03)

The Wendler version of the Torgov-Ananchenko scheme of total steroid synthesis was shown to be applicable to the preparation of 6-oxaestra-1,3.5(10), 8,14-pentaenes. Conditions for cyclodehydration of secosteroids thus obtained were found, which ensured i

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