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Benzenemethanamine, N-(phenylmethyl)-a-[(phenylseleno)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

730907-48-9

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730907-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 730907-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,0,9,0 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 730907-48:
(8*7)+(7*3)+(6*0)+(5*9)+(4*0)+(3*7)+(2*4)+(1*8)=159
159 % 10 = 9
So 730907-48-9 is a valid CAS Registry Number.

730907-48-9SDS

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 N-benzyl-1-phenyl-2-(phenylselanyl)ethan-1-amine

1.2 Other means of identification

Product number -
Other names Benzyl-(1-phenyl-2-phenylselanyl-ethyl)-amine

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:730907-48-9 SDS

730907-48-9Downstream Products

730907-48-9Relevant academic research and scientific papers

Visible-light-induced oxidative coupling of vinylarenes with diselenides leading to α-aryl and α-alkyl selenomethyl ketones

Liu, Gong-Qing,Yi, Wei,Wang, Peng-Fei,Liu, Ji,Ma, Meng,Hao, Da-Yun,Ming, Liang,Ling, Yong

, p. 1840 - 1846 (2021/03/09)

A visible-light-induced oxidative coupling of diselenides with readily available vinylarenes is demonstrated. This benign protocol allows one to access a wide range of α-aryl and α-alkyl selenomethyl ketones in good yields with excellent functional group compatibility. The distinct advantages of this protocol over all previous methods include the use of a green solvent and air as an oxidant and the lack of a photocatalyst, a base, and an oxidant as well as better green chemistry matrices. Furthermore, the title reaction can be performed with natural sunlight, the most sustainable energy source imaginable. Additionally, the mild reaction conditions, easy operation and suitability for the modification of styrene-functionalized biomolecules make the current reaction system a more attractive method for the synthesis of a variety of medicinal and agrochemical compounds of interest.

α-Phenylselanyl imines: Preparation of β-phenylselanyl amines and original synthesis of allylaziridines

Miniejew, Catherine,Outurquin, Francis,Pannecoucke, Xavier

, p. 447 - 456 (2007/10/03)

Resorting to suitable methods, a wide variety of α-phenylselanyl imines 2-5 were prepared from α-phenylselanyl aldehydes and α-phenylselanyl ketones 1. These compounds were reduced to afford β-phenylselanyl amines 6-9. Our experimental conditions have lim

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