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N-benzyl-1,2-dihydroisoquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104889-68-1

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104889-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104889-68-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,8 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104889-68:
(8*1)+(7*0)+(6*4)+(5*8)+(4*8)+(3*9)+(2*6)+(1*8)=151
151 % 10 = 1
So 104889-68-1 is a valid CAS Registry Number.

104889-68-1SDS

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 N-benzyl-1,2-dihydroisoquinoline

1.2 Other means of identification

Product number -
Other names 2-benzyl-1,2-dihydro-isoquinoline

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:104889-68-1 SDS

104889-68-1Relevant academic research and scientific papers

Transfer hydrogenation of isoquinolinium salts catalyzed by a rhodium complex

Wu, Jiashou,Liao, Jian,Zhu, Jin,Deng, Jingen

, p. 2059 - 2062 (2006)

Regio- and chemoselective transfer hydrogenation of isoquinolinium salts catalyzed by [Cp*RhCl2]2 using HCOOH-Et3N (5:2) as a hydrogen source was realized. A variety of N-methyl- and N-benzyl-1,2,3,4-tetrahydroisoquinoline

One-Pot Olefin Isomerization/Aliphatic Enamine Ring-Closing Metathesis/Oxidation/1,3-Dipolar Cycloaddition for the Synthesis of Isoindolo[1,2-a]isoquinolines

Fujii, Yuki,Takehara, Tsunayoshi,Suzuki, Takeyuki,Fujioka, Hiromichi,Shuto, Satoshi,Arisawa, Mitsuhiro

, p. 4055 - 4062 (2016/01/25)

N-Alkyl-N-(2-vinylbenzyl)prop-2-en-1-amine derivatives undergo a one-pot olefin isomerization/aliphatic enamine ring-closing metathesis (RCM)/oxidation/1,3-dipolar cycloaddition sequence with the ruthenium complex, Ru(CO)HCl(PPh3)3, a second generation Hoveyda-Grubbs catalyst, and a 1,3-dipolarophile. Overall, in a single operation the reaction sequence converts simple benzylamine derivatives into isoindolo[1,2-a]isoquinolines with a π-conjugated four-ring system, through three unique ruthenium-catalyzed transformations.

STEREOCHIMIE DE LA CYCLOADDITION DES DIARYLNITRILIMINES SUR LES N-ALKYL ET LES DIALKYL-1,2 DIHYDRO-1,2 ISOQUINOLEINES

Kitane, Said,Tshiamala, Kabula,Laude, Bernard,Vebrel, Joeel,Cerutti, Ernest

, p. 3737 - 3751 (2007/10/02)

The PMR spectroscopic properties (60 MHz) of cycloadducts of diarylnitrilimins towards 1,2-dihydroisoquinolines mono alkylated at the N-atom or dialkylated at the C1-carbon and N-atoms have been studied.Date allow us to determine the stereochemistry of th

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