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10166-05-9

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10166-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10166-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,6 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10166-05:
(7*1)+(6*0)+(5*1)+(4*6)+(3*6)+(2*0)+(1*5)=59
59 % 10 = 9
So 10166-05-9 is a valid CAS Registry Number.

10166-05-9SDS

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 4-benzylisoquinoline

1.2 Other means of identification

Product number -
Other names 4-Benzylisochinolin

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:10166-05-9 SDS

10166-05-9Relevant articles and documents

-

Badr,M.Z.A.,El-Sherief,H.A.H.

, p. 3831 - 3836 (1975)

-

Synthesis of isoquinolines and pyridines via palladium-catalysed iminoannulation of allenes

Diederen, Jeroen J. H.,Sinkeldam, Rene W.,Fruehauf, Hans-W,Hiemstra, Henk,Vrieze, Kees

, p. 4255 - 4258 (1999)

Various isoquinolines and pyridines were prepared from aryl- and vinyl halides by a method which involves insertion of an allene into the Pd-C bond and intramolecular nucleophilic attack of the imine.

Microwave-Assisted Palladium-Catalyzed Reductive Cyclization/Ring-Opening/Aromatization Cascade of Oxazolidines to Isoquinolines

Xu, Xianjun,Feng, Huangdi,Van Der Eycken, Erik V.

, p. 6578 - 6582 (2021/09/02)

An efficient palladium-catalyzed reaction of N-propargyl oxazolidines for the construction of 4-substituted isoquinolines under microwave irradiation is developed. This transformation proceeds through a sequential palladium-catalyzed reductive cyclization/ring-opening/aromatization cascade via C-O and C-N bond cleavages of the oxazolidine ring. The practical value of this method has also been explored by conducting a millimole-scale reaction, as well as by transforming the isoquinoline into a key intermediate for the synthesis of a lamellarin analogue.

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