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C25H29NO3 is a chemical compound with a molecular formula indicating it contains 25 carbon atoms, 29 hydrogen atoms, 1 nitrogen atom, and 3 oxygen atoms. C25H29NO3 has a molecular weight of approximately 393.5 g/mol. It is an organic molecule, likely a derivative of a larger class of compounds such as alkaloids or complex lipids, given its structure. The presence of nitrogen and oxygen suggests it may have functional groups like amines or carboxylic acids, which could influence its reactivity and properties. C25H29NO3 could be found in various applications, such as pharmaceuticals, due to its complex structure and potential biological activity.

3941-92-2

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3941-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3941-92-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,4 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3941-92:
(6*3)+(5*9)+(4*4)+(3*1)+(2*9)+(1*2)=102
102 % 10 = 2
So 3941-92-2 is a valid CAS Registry Number.

3941-92-2Upstream product

3941-92-2Downstream Products

3941-92-2Relevant academic research and scientific papers

Design and synthesis of KNT-127, a δ-opioid receptor agonist effective by systemic administration

Nagase, Hiroshi,Nemoto, Toru,Matsubara, Ayaka,Saito, Manabu,Yamamoto, Naoshi,Osa, Yumiko,Hirayama, Shigeto,Nakajima, Mayumi,Nakao, Kaoru,Mochizuki, Hidenori,Fujii, Hideaki

scheme or table, p. 6302 - 6305 (2010/11/18)

We have reported previously the novel δ-opioid agonist, SN-28, which was more potent in in vitro assays than the prototype δ-agonists, TAN-67 and SNC-80. However, when administered by subcutaneous injection, this compound showed no analgesic effect at dosages greater than 30 mg/kg in the acetic acid writhing test. We speculated that SN-28 was not effective in the test because the presence of the charged ammonium groups prevented its penetration through the blood-brain barrier. On the basis of our proposal, we designed the novel δ-agonist, KNT-127, which was effective with systemic administration.

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