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890-51-7

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890-51-7 Usage

Chemical Properties

yellow crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 890-51-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 890-51:
(5*8)+(4*9)+(3*0)+(2*5)+(1*1)=87
87 % 10 = 7
So 890-51-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H13N/c1-2-7-14(8-3-1)13-18-17-12-6-10-15-9-4-5-11-16(15)17/h1-13H/b18-13+

890-51-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-naphthalen-1-yl-1-phenylmethanimine

1.2 Other means of identification

Product number -
Other names N-benzylidenenaphthylamine

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:890-51-7 SDS

890-51-7Relevant articles and documents

Surfactant dependent pH controlled "off-on", "off-on-off" and "on-off" fluorescent switches exhibited by N-benzylidenenaphthalen-1-amine

Kumar, Jutika,Sarma, Manas Jyoti,Phukan, Prodeep,Das, Diganta Kumar

, p. 1431 - 1435 (2015)

N-benzylidenenaphthalen-1-amine (L) acts as pH dependent "off-on", "off-on-off" and "on-off" fluorescent switch in 1:1 (v/v) CH3CN:H2O depending on the presence of anionic sodiumdocdecyl sulphate (SDS), neutral triton X-100 (TX-100)

Copper-Catalyzed Intramolecular Amination of C(sp3)-H Bond of Secondary Amines to Access Azacycles

Jin, Ruo-Xing,Dai, Jing-Cheng,Li, Yan,Wang, Xi-Sheng

supporting information, p. 421 - 426 (2021/01/26)

The cross-coupling of C-N bond directly from inert C-H bonds is an ideal approach to synthesize saturated azacycles due to its high efficiency and atom economy. In this article, a copper-catalyzed intramolecular amination via the cross coupling of C(sp3)-H and N-H bonds of secondary amine has been reported, which exhibit excellent chemo- and regioselectivity, extensive substrate scope, and functional group tolerance in good to excellent yield, offering an efficient pathway to build nitrogen-containing heterocycle skeletons.

Catalyst- And Solvent-Free Synthesis of α-Amino Polyfluoroalkylphosphonates from Bis(fluoroalkyl) Phosphonates and Aldimines

Arbuzova, Svetlana N.,Gusarova, Nina K.,Kazantseva, Tatyana I.,Kolyvanov, Nikita A.,Trofimov, Boris A.,Verkhoturova, Svetlana I.,Zinchenko, Sergey V.

, p. 1531 - 1540 (2020/05/19)

The catalyst- and solvent-free reaction between bis(fluoroalkyl) phosphonates and aldimines occurs under mild conditions (20-22 °C, 0.25-4 h) to afford a new family of α-amino polyfluoroalkylphosphonates in up to quantitative yields.

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