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1,2-Ethanediamine, N-(phenylmethyl)-N'-[2-[(phenylmethyl)amino]ethyl]-, trihydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17327-82-1

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17327-82-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17327-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,2 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17327-82:
(7*1)+(6*7)+(5*3)+(4*2)+(3*7)+(2*8)+(1*2)=111
111 % 10 = 1
So 17327-82-1 is a valid CAS Registry Number.

17327-82-1Relevant articles and documents

Multigram four-step synthesis of 1,4,7-triazacyclononanes with 2Ra/Rb N-functionalization pattern by starting from diethylenetriamine

Gros, Guillaume,Hasserodt, Jens

, p. 183 - 187 (2015)

Polyazamacrocycles and their derivatives are appreciated for the strength of their corresponding metal complexes. 1,4,7-Triazacyclononane (TACN) derivatives have been employed in an ever increasing number of applications. To this day, all synthetic routes to TACN derivatives that have identical or differing substituents require the initial preparation of unprotected TACN. Herein, we report the four-step synthesis of TACN derivatives that have a 2Ra/Rb N-functionalization pattern by starting from diethylenetriamine and employing an organic template strategy.

Direct access to terpyridine-containing polyazamacrocycles as photosensitizing ligands for Eu(III) luminescence in aqueous media

Galaup, Chantal,Couchet, Jean-Marc,Bedel, Sebastien,Tisnes, Pierre,Picard, Claude

, p. 2274 - 2284 (2007/10/03)

(Chemical Equation Presented) The synthesis of new 18-membered hexaazamacrocycles containing a functionalized 2,2′:6′,2″- terpyridine moiety as part of the cyclic backbone and three acetate pendant arms is described. The reported synthetic procedure is ba

Antiaggregatory and anticoagulant effects of oligoamines. 12. Alkyl- and arylalkyl- derivatives of putrescine, spermidine and spermine

Rehse,Puchert,Leissring

, p. 287 - 294 (2007/10/02)

Eleven lipophilic derivatives of the title biogenic amines and 28 structurally related triamines and tetramines have been synthesized. Twenty-three of them inhibited the platelet aggregation induced by collagen at an IC50 between 8 mumol/L and 30 mumol/L. Five compounds prolonged the one stage thromboplastin time (Quick) by 7s or more at 100 mumol/L. The antiplatelet and anticoagulant effect do not run parallel. The relationship between the effects observed and the chemical structure of the oligoamines has been elucidated.

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