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3-methoxy-N-(4-methoxyphenyl)-4-methylaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36661-35-5

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36661-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36661-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,6 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36661-35:
(7*3)+(6*6)+(5*6)+(4*6)+(3*1)+(2*3)+(1*5)=125
125 % 10 = 5
So 36661-35-5 is a valid CAS Registry Number.

36661-35-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxy-N-(4-methoxyphenyl)-4-methylaniline

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

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

More Details:36661-35-5 SDS

36661-35-5Relevant academic research and scientific papers

Transition metals in organic synthesis, part 91:1 palladium-catalyzed approach to 2,6-dioxygenated carbazole alkaloids - First total synthesis of the phytoalexin carbalexin C

Schmidt, Marika,Kn?lker, Hans-Joachim

body text, p. 2421 - 2424 (2010/01/07)

The palladium(0)-catalyzed C-N bond formation and palladium(II)-catalyzed oxidative cyclization provide an efficient route to a series of 2,6-dioxygenated carbazole alkaloids including the first total synthesis of the phytoalexin carbalexin C.

Acid-free synthesis of carbazoles and carbazolequinones by intramolecular Pd-catalyzed, microwave-assisted oxidative biaryl coupling reactions efficient syntheses of murrayafoline A, 2-methoxy-3-methylcarbazole, and glycozolidine

Sridharan, Vellaisamy,Antonia Martin,Carlos Menendez

supporting information; experimental part, p. 4614 - 4621 (2009/12/05)

A mild and. efficient methodology for the synthesis of oxygenated. carbazoles from diarylamines under non-acidic conditions was developed, based on a palladium-catalyzed, microwave-assisted double C-H bond activation process. This new protocol was successfully applied to the synthesis of three naturally occurring carbazoles, namely murrayafoline A, 2-methoxy-3-methylcarbazole, and glycozolidine. The scope of the reaction was also expanded, to include the synthesis of benzo fused carbazolequinones. Wiley-VCH Verlag GmbH & Co. KGaA.

Thermal cyclisation of diphenylamine to carbazole: Synthesis of the natural product glycozolidine

Islam,Bhattacharyya,Chakraborty

, p. 537a (2007/10/04)

Iodine-catalysed cyclisation at 350 °C of diphenylamine to carbazole has been used to synthesise glycozolidine (VI), a natural product from Glycosmis pentaphylla (Retz.) D.C.

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