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Benzeneethanamine, N,N-dibutyl-a-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59313-94-9

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59313-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59313-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,1 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59313-94:
(7*5)+(6*9)+(5*3)+(4*1)+(3*3)+(2*9)+(1*4)=139
139 % 10 = 9
So 59313-94-9 is a valid CAS Registry Number.

59313-94-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-di-n-butylnamphetamine

1.2 Other means of identification

Product number -
Other names Dibutyl-(1-methyl-2-phenyl-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:59313-94-9 SDS

59313-94-9Downstream Products

59313-94-9Relevant academic research and scientific papers

Practical Catalytic Cleavage of C(sp3)?C(sp3) Bonds in Amines

Li, Wu,Liu, Weiping,Leonard, David K.,Rabeah, Jabor,Junge, Kathrin,Brückner, Angelika,Beller, Matthias

supporting information, p. 10693 - 10697 (2019/07/09)

The selective cleavage of thermodynamically stable C(sp3)?C(sp3) single bonds is rare compared to their ubiquitous formation. Herein, we describe a general methodology for such transformations using homogeneous copper-based catalysts in the presence of air. The utility of this novel methodology is demonstrated for Cα?Cβ bond scission in >70 amines with excellent functional group tolerance. This transformation establishes tertiary amines as a general synthon for amides and provides valuable possibilities for their scalable functionalization in, for example, natural products and bioactive molecules.

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