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The chemical compound "N'-(8-chloro-1H-benzo[e][1,4]diazepin-5-yl)-N,N-diethyl-ethane-1,2-diamine" is a complex organic molecule with a molecular formula of C16H22ClN3. It features a benzo[e][1,4]diazepine ring system, which is a fused ring structure consisting of a benzene ring and two nitrogen atoms forming a diazepine ring. The 8-chloro substitution on the benzo[e][1,4]diazepine ring introduces a chlorine atom at the 8th position, which can significantly alter the compound's physical and chemical properties. The molecule also contains an ethane-1,2-diamine moiety, which is a chain of two carbon atoms with an amine group attached to each end. The N,N-diethyl groups attached to the nitrogen atoms of the ethane-1,2-diamine part of the molecule contribute to its lipophilicity and may influence its reactivity and solubility. N'-(8-chloro-1H-benzo[e][1,4]diazepin-5-yl)-N,N-diethyl-ethane-1,2-diamine is likely to be used in pharmaceutical or chemical research due to its unique structure and potential for interaction with biological targets.

69063-12-3

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69063-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69063-12-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,6 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69063-12:
(7*6)+(6*9)+(5*0)+(4*6)+(3*3)+(2*1)+(1*2)=133
133 % 10 = 3
So 69063-12-3 is a valid CAS Registry Number.

69063-12-3Downstream Products

69063-12-3Relevant academic research and scientific papers

Photolysis of Quinolyl and Isoquinolyl Azides in Primary and Secondary Aliphatic Amines: Synthesis of Bicyclic Azepines, Diazepines, and Quinolyl- and Isoquinolyl-diamines

Hollywood, Frank,Nay, Barry,Scriven, Eric F. V.,Suschitzky, Hans,Khan, Zafar U.,Hull, Roy

, p. 421 - 429 (2007/10/02)

Photolysis of the title compounds in primary aliphatic amines gave in some cases bicyclic azepines and diazepines as well as o-diamines, while in secondary amines mainly the appropriate o-diamines are obtained.On the basis of the many examples studied guidelines are put forward to predict the nature of products from photolysis of bicyclic azides in primary and secondary amines and to obtain maximum yields.

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