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BENZAMIDINE, N-ALLYL-N-(p-(2-(DIISOPROPYLAMINO)ETHOXY)PHENYL)- is a complex organic compound with the chemical formula C21H28N2O. It is a derivative of benzamidine, featuring an allyl group attached to the nitrogen atom and a p-(2-diisopropylamino)ethoxyphenyl group connected to the other nitrogen atom. BENZAMIDINE, N-ALLYL-N-(p-(2-(DIISOPROPYLAMINO)ETHOXY)PHENYL)- is characterized by its unique molecular structure, which may have potential applications in various chemical and pharmaceutical industries. Due to its specific functional groups, it could be involved in the synthesis of other complex molecules or used as a building block in the development of new drugs. However, further research and analysis are required to fully understand its properties and potential uses.

80784-92-5

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80784-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80784-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,8 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80784-92:
(7*8)+(6*0)+(5*7)+(4*8)+(3*4)+(2*9)+(1*2)=155
155 % 10 = 5
So 80784-92-5 is a valid CAS Registry Number.

80784-92-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-[2-[di(propan-2-yl)amino]ethoxy]phenyl]-N'-prop-2-enylbenzenecarboximidamide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:80784-92-5 SDS

80784-92-5Downstream Products

80784-92-5Relevant academic research and scientific papers

Chemistry and hypoglycemic activity of N[[(dialkylamino)alkoxy]phenyl]benzamidines

Shroff,Elpern,Kobrin,Cervoni

, p. 359 - 362 (2007/10/02)

A series of N-[[(dialkylamino)alkoxy]phenyl]benzamidines was synthesized and evaluated for hypoglycemic activity in the glucose-primed rat. Structure-activity relationships indicated r117w1 =N1-phenyl-N-[4[2-(diisopropylamino)-ethox]phenyl]benzamid ine that N'-phenyl-N-[2-(diisopropylamino)-ethoxy]phenyl]benzamidine hydrobromide, N'-(4-chlorophenyl)-N-[4-(diisopropylamino)ethoxy]phenyl]-bensamidine dihydrochloride, and N'-phenyl-N-[4-[(diisopropylamino)propoxy]phenyl]benzamidine dihydrobromide are some of the more interesting compounds. A comparison of these hypoglycemic agents with classical standards (tolazamide, phenformin, and buformin) in several experimental models showed that the benzamidines seem to combine in one molecule some of the biological activities of the β-cytotrophic sulfonylureas and some of the activities of the biguanides.

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