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1-Methoxy-9-[(1-methoxy-9H-carbazol-3-yl)methyl]-3-methyl-9H-carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89368-89-8

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89368-89-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89368-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,6 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89368-89:
(7*8)+(6*9)+(5*3)+(4*6)+(3*8)+(2*8)+(1*9)=198
198 % 10 = 8
So 89368-89-8 is a valid CAS Registry Number.

89368-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name bismurrayafoline-A

1.2 Other means of identification

Product number -
Other names 1-methoxy-9-[(1-methoxycarbazol-3-yl)-methyl]-3-methylcarbazole

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:89368-89-8 SDS

89368-89-8Downstream Products

89368-89-8Relevant academic research and scientific papers

Synthesis of Methylene-Bridged Biscarbazole Alkaloids by using an Ullmann-type Coupling: First Total Synthesis of Murrastifoline-C and Murrafoline-E

Kutz, Sebastian K.,B?rger, Carsten,Schmidt, Arndt W.,Kn?lker, Hans-Joachim

, p. 2487 - 2500 (2016/02/14)

We describe the total synthesis of methylene-bridged biscarbazole alkaloids by using a late-stage Ullmann-type coupling of fully functionalised carbazole subunits. The carbazole derivatives were synthesised via a sequence of palladium(0)- and palladium(II

First total syntheses of chrestifoline-B and (±)-chrestifoline-C, and improved synthetic routes to bismurrayafoline-A, bismurrayafolinol and chrestifoline-D

Boerger, Carsten,Schmidt, Arndt W.,Knoelker, Hans-Joachim

, p. 3831 - 3835 (2014/06/09)

We describe an efficient synthesis of the methylene-bridged biscarbazole alkaloids bismurrayafoline-A, bismurrayafolinol and chrestifoline B-D using an Ullmann-type coupling at the benzylic position. This journal is the Partner Organisations 2014.

Novel approach to biscarbazole alkaloids via Ullmann coupling - Synthesis of murrastifoline - A and bismurrayafoline - A

B?rger, Carsten,Kataeva, Olga,Kn?lker, Hans-Joachim

, p. 7269 - 7273 (2012/10/07)

Unprecedented Ullmann couplings of murrayafoline-A with either 6-bromo- or 4-bromocarbazole derivatives provide highly efficient synthetic routes to the biscarbazole alkaloids murrastifoline-A (6 steps, 66% overall yield) and bismurrayafoline-A (6 steps, 28% overall yield).

Synthesis of methylene-bridged binary carbazole alkaloids and a related tricarbazole

Bringmann, Gerhard,Tasler, Stefan

, p. 2337 - 2343 (2007/10/03)

The first synthesis of the methylene-bridged binary carbazole alkaloids bismurrayafoline-A and chrestifoline-A is described. As an interesting side product, a likewise benzylically connected trimer was identified, a potential natural product.

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