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Benzeneethanamine, b-methylene-N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123974-18-5

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123974-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123974-18-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,9,7 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 123974-18:
(8*1)+(7*2)+(6*3)+(5*9)+(4*7)+(3*4)+(2*1)+(1*8)=135
135 % 10 = 5
So 123974-18-5 is a valid CAS Registry Number.

123974-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-2-phenyl-2-propen-1-amine

1.2 Other means of identification

Product number -
Other names N-benzyl-2-phenyl-2-propenamine

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:123974-18-5 SDS

123974-18-5Relevant academic research and scientific papers

A convenient method for the synthesis of β,γ-unsaturated amines from alkenes via α,β-unsaturated diphenylsulfonium salts

Yamanaka, Hiroyuki,Matsuo, Jun-Ichi,Kawana, Asahi,Mukaiyama, Teruaki

, p. 626 - 627 (2003)

1,1-Disubstituted and trisubstituted alkenes were converted into the corresponding β,γ-unsaturated amines 4 via three steps: the initial formation of α,β-unsaturated diphenylsulfonium triflates 2 from alkenes and diphenyl(trifluoromethanesulfonyloxy)sulfo

CF2-containing 2-oxazoline ketone compounds and preparation method thereof

-

, (2018/04/01)

The invention provides a method for mildly and efficiently compounding a series of CF2-containing 2-oxazoline ketone compounds under a photocatalysis condition by actively combining difluoroalkylationreaction with carbon dioxide. The method provided by th

Anti-Markovnikov rearrangement in sulfur mediated allylic C-H amination of olefins

Zhang, Zhong,Du, Hongguang,Xu, Jiaxi,Li, Pingfan

supporting information, p. 11547 - 11550 (2016/10/03)

Cationic rearrangement reactions usually follow Markovnikov's rule to give more substituted carbocations as stable intermediates. During our study on sulfur mediated allylic C-H amination of olefins, very rare cases of anti-Markovnikov rearrangement from secondary carbocations toward primary carbocations or primary triflates were observed.

2-Arylallyl as a new protecting group for amines, amides and alcohols

Barluenga, Jose,Fananas, Francisco J.,Sanz, Roberto,Marcos, Cesar,Ignacio, Jose M.

, p. 933 - 935 (2007/10/03)

Amines, amides and ethers containing 2-arylallyl groups are selectively and easily deprotected with tert-butyllithium. This transformation probably involves a carbolithiation reaction of the styrenyl moiety followed by a β-elimination process. The Royal Society of Chemistry 2005.

SYNTHESIS OF DERIVATIVES OF 3-HYDROXYMETHYL-3-PHENYLAZETIDINE AND ATTEMPTED CONVERSIONS TO 3-PHENYL-1-AZABICYCLOPENTANE OR 3-PHENYL-1-AZABICYCLOHEXANE

Anderson, Arthur G.,Jewell, Richard A.

, p. 81 - 86 (2007/10/02)

The synthesis of eleven new derivatives of 3-hydroxymethyl-3-phenylazetidine and attempts to form the corresponding 1-azabicyclopentane or 1-azabicyclostructure from these are described.

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