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1-Propanamine, 2,2-dimethyl-N-(phenylmethylene)-, also known as 2,2-dimethyl-N-(phenylmethylene)propan-1-amine, is an organic compound with the chemical formula C11H17N. It is a derivative of propanamine, featuring a phenylmethylene group attached to the nitrogen atom. 1-Propanamine, 2,2-dimethyl-N-(phenylmethylene)- is characterized by its amine functional group, which is a primary amine due to the presence of one alkyl group attached to the nitrogen. It is a colorless liquid with a pungent odor and is used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. The compound is also known by several other names, including 2,2-dimethyl-N-(phenylmethylene)propan-1-amine, which highlights its structural features.

7731-35-3

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7731-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7731-35-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,3 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7731-35:
(6*7)+(5*7)+(4*3)+(3*1)+(2*3)+(1*5)=103
103 % 10 = 3
So 7731-35-3 is a valid CAS Registry Number.

7731-35-3SDS

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-(2,2-dimethylpropyl)-1-phenylmethanimine

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7731-35-3 SDS

7731-35-3Relevant academic research and scientific papers

Expanding Coefficient: A Parameter to Assess the Stability of Induced-Fit Complexes

Talotta, Carmen,Concilio, Gerardo,De Rosa, Margherita,Soriente, Annunziata,Gaeta, Carmine,Rescifina, Antonio,Ballester, Pablo,Neri, Placido

supporting information, p. 1804 - 1808 (2021/03/08)

Here we propose a new parameter, the Expanding Coefficient (EC), that can be correlated with the thermodynamic stability of supramolecular complexes governed by weak secondary interactions and obeying the induced-fit model. The EC values show a good linear relationship with the log Kapp of the respective pseudorotaxane complexes investigated. According to Cram's Principle of Preorganization, the EC can be considered an approximate mechanical measure of the host's reorganization energy cost upon adopting the final bound geometry.

A metallopeptoid as an efficient bioinspired cooperative catalyst for the aerobic oxidative synthesis of imines

Chandra Mohan, Darapanani,Sadhukha, Arghya,Maayan, Galia

, p. 139 - 144 (2017/10/16)

Enzymatic catalysis is largely based on intramolecular cooperativity between a metal center and functional organic molecules located on one scaffold. Inspired by this concept we have designed the metallopeptoid trimer BT, which is a unique intramolecular cooperative oxidation catalyst incorporating two catalytic centers, phenanthroline-copper and TEMPO, as well as one non-catalytic benzyl group. Herein we explore the capability of BT to act as an efficient catalyst for the oxidative synthesis of imines, which are versatile intermediates in the fine chemicals and pharmaceutical industries. We demonstrate that BT, combined with CuI, can catalyze the production of benzyl, aryl, heteroaryl, allylic and aliphatic imines from various alcohols and amines with a turn-over-number up to 45 times higher than this achieved when phenanthroline, copper and TEMPO are mixed in solution. Moreover, in low catalyst(s) loading, BT enables transformations that are not possible when a mixture of the individual catalysts is employed.

Factors influencing the regioselectivity of the oxidation of asymmetric secondary amines with singlet oxygen

Ushakov, Dmitry B.,Plutschack, Matthew B.,Gilmore, Kerry,Seeberger, Peter H.

supporting information, p. 6528 - 6534 (2015/04/22)

Aerobic amine oxidation is an attractive and elegant process for the α functionalization of amines. However, there are still several mechanistic uncertainties, particularly the factors governing the regioselectivity of the oxidation of asymmetric secondary amines and the oxidation rates of mixed primary amines. Herein, it is reported that singlet-oxygen-mediated oxidation of 1° and 2° amines is sensitive to the strength of the α-C-H bond and steric factors. Estimation of the relative bond dissociation energy by natural bond order analysis or by means of one-bond C-H coupling constants allowed the regioselectivity of secondary amine oxidations to be explained and predicted. In addition, the findings were utilized to synthesize highly regioselective substrates and perform selective amine cross-couplings to produce imines.

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