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4-phenyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione is a complex organic compound belonging to the class of benzodiazepines. This molecule features a benzene ring fused to a diazepine ring, with a phenyl group attached to the 4-position of the diazepine. The compound has two carbonyl groups at the 2 and 5 positions, indicating the presence of two ketone functional groups. This specific structure classifies it as a dihydro derivative, meaning it contains one less hydrogen atom than the fully saturated parent compound. Benzodiazepines are known for their various pharmacological properties, including sedative, hypnotic, and anxiolytic effects. However, the specific biological activity and potential applications of 4-phenyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione have not been extensively studied, and further research is needed to understand its potential therapeutic uses and safety profile.

1843-55-6

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1843-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1843-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1843-55:
(6*1)+(5*8)+(4*4)+(3*3)+(2*5)+(1*5)=86
86 % 10 = 6
So 1843-55-6 is a valid CAS Registry Number.

1843-55-6Downstream Products

1843-55-6Relevant academic research and scientific papers

Solvent-free synthesis of novel benzodiazepine derivatives by a three-component base-catalysed reaction of isatoic anhydride, a primary amine and chloroacetyl chloride

Seydey, Mohsen Khalilpour,Rezaei, Zahra,Homami, Seyed Saied

, p. 286 - 288 (2015/06/02)

Heating isatoic anhydride with a series of primary amines at 150 °C under solvent-free conditions yielded 2-amino-N-alkylbenzamides which, in the same pot, reacted readily with chloroacetyl chloride in the presence of poly(dimethylaminoethyl acrylamide)-modified magnetic nanoparticles (MNP@PDMA), a base catalyst, to give 4-alkyl-1,4-benzodiazepine-2,5-diones in good yields without formation of by-products.

A new entry to [1,2,4]triazolo[1,5-α][1,4]benzodiazepin-6-ones via intramolecular nitrilimine cycloaddition to the cyano group

Broggini, Gianluigi,Garanti, Luisa,Molteni, Giorgio,Zecchi, Gaetano

, p. 14859 - 14868 (2007/10/03)

A series of [1,2,4]triazolo[1,5-α][1,4]benzodiazepin-6-ones of potential pharmacological interest have been synthesised by means of intramolecular nitrilimine cycloadditions to the cyano group.

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