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3-tert-butyl-9-methyl-2,3,4,9-tetrahydro-1H-carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22401-72-5

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22401-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22401-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,0 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22401-72:
(7*2)+(6*2)+(5*4)+(4*0)+(3*1)+(2*7)+(1*2)=65
65 % 10 = 5
So 22401-72-5 is a valid CAS Registry Number.

22401-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-tert-butyl-9-methyl-1,2,3,4-tetrahydrocarbazole

1.2 Other means of identification

Product number -
Other names 3-tert.Butyl-9-methyl-tetrahydrocarbazol

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:22401-72-5 SDS

22401-72-5Downstream Products

22401-72-5Relevant academic research and scientific papers

An Electrophilic Bromine Redox Catalysis for the Synthesis of Indole Alkaloid Building Blocks by Selective Aliphatic C?H Amination

Bergès, Julien,García, Belén,Mu?iz, Kilian

supporting information, p. 15891 - 15895 (2018/11/23)

A new homogeneous bromine(?I/I) redox catalysis is described, which is based on monomeric bromine(I) compounds containing transferable phthalimidato groups. These catalysts enable intermolecular C?H amination reactions at previously unaccessible aliphatic positions and thus enlarge the synthetic potential of direct C?N bond formation, including its application in the synthesis of alkaloid building blocks. This aspect is demonstrated by a new synthetic approach to aspidospermidine. In addition to the development of the catalyst system, the structures of the involved bromine(I) key catalysts were fully elucidated, including by X-ray analyses.

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