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1H-Indene-2-carbothioamide, N-(4-bromophenyl)-3-(4-morpholinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32281-91-7

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32281-91-7 Usage

Chemical Class

Sulfamide derivative

Molecular Weight

407.26 g/mol

Physical Appearance

White crystalline solid

Solubility

Soluble in DMSO, poorly soluble in water

Mechanism of Action

Selective inhibitor of receptor-operated calcium channels (ROCCs); potent and selective blocker of TRPC channels

Therapeutic Applications

Potential treatment for hypertension, cardiac arrhythmias, and neurodegenerative diseases

Cellular Processes Modulation

Proliferation, migration, and apoptosis

Research Utility

Valuable tool for studying the role of calcium signaling in physiological and pathological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 32281-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,8 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32281-91:
(7*3)+(6*2)+(5*2)+(4*8)+(3*1)+(2*9)+(1*1)=97
97 % 10 = 7
So 32281-91-7 is a valid CAS Registry Number.

32281-91-7Relevant academic research and scientific papers

The Reaction of Malononitrile with Some Enamines of 1-Indanone. Synthesis of o-Aminonitriles of Indenopyridine and Indenothiopyran

Bogdanowicz-Szwed, Krystyna,Feret, Hanna,Lipowska, Malgorzata

, p. 623 - 627 (2007/10/02)

The reaction of enamines of 1-oxo-indan-2-carboxylic acid anilides (1) with malononitrile yielded 2-arylcarbamylindenylidene-malononitriles (3), which in alkaline solution underwent cyclization to indenopyridines (4).Enamines of 1-oxo-indan-2-carbothionic acid anilides (2) reacted with malononitrile yielding indenothiopyrans (6), which under influence of alkalis were transformed to indenopyridines (8). - Enamines of β-Ketoacid Anilides, o-Aminonitriles, Indenopyridine, Indenothiopyran

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