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[(10H-phenothiazin-10-ylcarbonyl)imino]diethane-2,1-diyl bis(methylcarbamate) is a bis(methylcarbamate) derivative of phenothiazine, a heterocyclic compound with a seven-membered ring containing two nitrogen atoms. It is known for its anthelmintic properties and is being explored for its potential as an anti-cancer and anti-inflammatory agent.

65240-98-4

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65240-98-4 Usage

Uses

Used in Veterinary Medicine:
[(10H-phenothiazin-10-ylcarbonyl)imino]diethane-2,1-diyl bis(methylcarbamate) is used as an anthelmintic drug for treating parasitic worm infections in animals. It works by inhibiting the activity of enzymes involved in energy metabolism and muscle function of parasites, leading to their paralysis and death.
Used in Pharmaceutical Research:
[(10H-phenothiazin-10-ylcarbonyl)imino]diethane-2,1-diyl bis(methylcarbamate) is used as a potential anti-cancer agent in preclinical studies. Its structure and properties make it an interesting target for further chemical modification and drug development, with promising results in the fight against cancer.
Used in Anti-Inflammatory Research:
[(10H-phenothiazin-10-ylcarbonyl)imino]diethane-2,1-diyl bis(methylcarbamate) is also being researched for its potential as an anti-inflammatory agent, due to its unique chemical structure and properties that may offer new avenues for treating inflammation-related conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 65240-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,4 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65240-98:
(7*6)+(6*5)+(5*2)+(4*4)+(3*0)+(2*9)+(1*8)=124
124 % 10 = 4
So 65240-98-4 is a valid CAS Registry Number.

65240-98-4Downstream Products

65240-98-4Relevant academic research and scientific papers

Phenothiazinealkaneamines for treatment of neurotoxic injury

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, (2008/06/13)

Compounds, compositions and methods of treatment are described to control brain damage associated with anoxia or ischemia which typically follows such conditions as stroke, cardiac arrest or perinatal asphyxia. The treatment includes administration of a phenothiazinealkaneamine compound as an antagonist to inhibit excitotoxic actions at major neuronal excitatory amino acid receptor sites. Compounds of most interest are those of the formula STR1 wherein each of R1 and R2 is hydrido; wherein each of R3 and R4 is independently selected from hydrido, methyl and ethyl; wherein each of R5 and R6 is independently selected from methyl, ethyl and n-propyl; wherein X is sulfur; wherein m is zero; and wherein n is two.

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