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2,3-dihydro-(2-phenylmethyl)-1H-benz[de]isoquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65448-54-6

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65448-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65448-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,4 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65448-54:
(7*6)+(6*5)+(5*4)+(4*4)+(3*8)+(2*5)+(1*4)=146
146 % 10 = 6
So 65448-54-6 is a valid CAS Registry Number.

65448-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydro-(2-phenylmethyl)-1H-benz[de]isoquinoline

1.2 Other means of identification

Product number -
Other names 2-Benzyl-2,3-dihydro-1H-benz[de]isochinolin

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65448-54-6 SDS

65448-54-6Relevant academic research and scientific papers

Synthesis, characterization, and coordination chemistry of the 2-azaphenalenyl radical

Zheng, Shijun,Lan, Jie,Khan, Saeed I.,Rubin, Yves

, p. 5786 - 5791 (2007/10/03)

The 2-azaphenalenyl radical 2 has been synthesized and characterized by ESR spectroscopy. Variable-temperature ESR measurements were carried out on both the phenalenyl (1) and the 2-azaphenalenyl (2) radicals. The phenalenyl radical 1 has the known propen

New and Convenient Synthesis of 2-Substituted 2,3-Dihydro-1H-benzisoquinolin-1-ones

Sato, Ryu,Oikawa, Katsuyuki,Goto, Takehiko,Saito, Minoru

, p. 2238 - 2240 (2007/10/02)

Various 2-substituted 2,3-dihydro-1H-benzisoquinolin-1-ones were obtained in high yields by chemoselective reduction of 2-substituted 1H-benzisoquinoline-1,3(2H)-diones with sodium or zinc borohydride at room temperature.

Inhibitors of Bllod Platelet Aggregation. Activity of Some 1H-Benzisoquinolinecarboximidamides on the in Vivo Blood Platelet Aggregation Induced by Collagen

Beetz, Tom,Meuleman, Dick G.,Wieringa, Joop H.

, p. 714 - 719 (2007/10/02)

A series of 33-1H-benzisoquinolinecarboximidamides has been prepared and tested in the rat after intraperitoneal (ip) and/or oral (po) administration for their ability to inhibit the in vivo blood platelet aggregation induced by colagen.In this aggregation test, a considerable number of active compounds were found.Fourteen compounds were active when administred ip , five of which also exhibited significant po activity.One compound was toxic after ip administration but was found to be active after po administration without apparent toxicity.Itis thought that the solubility of the drug in water is an important factor for the resorption after oral administration and, hence, for its oral activity.

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