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1H-Azepine, 1-(1-cyclohexen-1-yl)hexahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23430-63-9

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23430-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23430-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,3 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23430-63:
(7*2)+(6*3)+(5*4)+(4*3)+(3*0)+(2*6)+(1*3)=79
79 % 10 = 9
So 23430-63-9 is a valid CAS Registry Number.

23430-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohex-1-enyl-azepane

1.2 Other means of identification

Product number -
Other names 1-Hexamethylenimino-cyclohexen-(1)

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:23430-63-9 SDS

23430-63-9Relevant academic research and scientific papers

peri-Xanthenoxanthene (PXX): a Versatile Organic Photocatalyst in Organic Synthesis

Pezzetta, Cristofer,Folli, Andrea,Matuszewska, Oliwia,Murphy, Damien,Davidson, Robert W. M.,Bonifazi, Davide

supporting information, p. 4740 - 4753 (2021/04/09)

Recent years have witnessed a continuous development of photocatalysts to satisfy the growing demand of photophysical and redox properties in photoredox catalysis, with complex structures or alternative strategies devised to access highly reducing or oxidising systems. We report herein the use of peri-xanthenoxanthene (PXX), a simple and inexpensive dye, as an efficient photocatalyst. Its highly reducing excited state allows activation of a wide range of substrates, thus triggering useful radical reactions. Benchmark transformations such as the addition of organic radicals, generated by photoreduction of organic halides, to radical traps are initially demonstrated. More complex dual catalytic manifolds are also shown to be accessible: the β-arylation of cyclic ketones is successful when using a secondary amine as organocatalyst, while cross-coupling reactions of aryl halides with amines and thiols are obtained when using a Ni co-catalyst. Application to the efficient two-step synthesis of the expensive fluoro-tetrahydro-1H-pyrido[4,3-b]indole, a crucial synthetic intermediate for the investigational drug setipiprant, has been also demonstrated. (Figure presented.).

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