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2-Bromo-3,5,5-trimethyl-cyclohexanone is a chemical compound with the molecular formula C9H15BrO. It is a halogenated ketone derivative of cyclohexanone, featuring a bromine atom at the 2-position, and two methyl groups at the 3 and 5 positions. This organic compound is characterized by its cyclic structure and the presence of a carbonyl group, which is a carbon-oxygen double bond. It is a colorless to pale yellow liquid with a pungent odor and is soluble in organic solvents. Due to its reactivity, it is often used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound should be handled with care, as it can be harmful if inhaled, ingested, or absorbed through the skin, and it may also cause irritation to the eyes and respiratory system.

4883-54-9

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4883-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4883-54-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4883-54:
(6*4)+(5*8)+(4*8)+(3*3)+(2*5)+(1*4)=119
119 % 10 = 9
So 4883-54-9 is a valid CAS Registry Number.

4883-54-9Upstream product

4883-54-9Downstream Products

4883-54-9Relevant academic research and scientific papers

GUANIDINE DERIVATIVES AND USE THEREOF AS NEUROPEPTIDE FF RECEPTOR ANTAGONISTS

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Page 40, (2010/02/08)

The invention relates to guanidine derivatives of formula (I) where: A = a chain of 3-c6 carbon atoms, one of which can be replaced by -N(R')- or -O- and R' = H or a substituent, where the ring skeleton only contains both double bonds of the thiazole component, the pharmaceutically-acceptable acid addition salts of basic compounds of formula (I), the pharmaceutically-acceptable salts of compounds of formula (I),, comprising acid groups, with bases, the pharmaceutically-acceptable esters of hydroxy or carboxyl group containing compounds of formula (I) and the solvates or hydrates thereof, which are partly known and partly novel and exhibit a neuropeptide FF receptor antagonist effect. The above are suitable for the treatment of pain and hyperalgesia, withdrawal symptoms in alcohol, psychotropic and nicotine dependencies, for improvement or cure of said dependencies, for regulation of insulin excretion, food intake, memory functions, blood pressure, electrolyte and energy management and for treatment of urinary incontinence. The above can be produced using generally used methods and processed to give medicaments.

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