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18263-29-1

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18263-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18263-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,6 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18263-29:
(7*1)+(6*8)+(5*2)+(4*6)+(3*3)+(2*2)+(1*9)=111
111 % 10 = 1
So 18263-29-1 is a valid CAS Registry Number.

18263-29-1SDS

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 1-naphthalen-2-yl-N-phenylmethanimine

1.2 Other means of identification

Product number -
Other names 2-naphthylmethylideneaniline

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:18263-29-1 SDS

18263-29-1Relevant articles and documents

Synthesis, structure and catalytic polymerization activity of half-sandwich cyclometallated iridium complexes

Yao, Zi-Jian,Li, Peng,Li, Kuan,Deng, Wei

, (2018)

A series of mononuclear half-sandwich cyclometallated iridium complexes with Schiff base ligands were synthesized in good yields. Five air-stable C,N-chelate mode complexes were obtained smoothly through metal-mediated C─H bond activation. Treatments of d

-

Schulze et al.

, p. 428,438 (1961)

-

Rhodium catalyzed multicomponent dehydrogenative annulation: one-step construction of isoindole derivatives

Cheng, Biao,Lyu, Hairong,Quan, Yangjian,Xie, Zuowei

supporting information, p. 7930 - 7933 (2021/08/17)

A strategy for one-pot synthesis of isoindoles is describedviaa catalytic multicomponent dehydrogenative annulation of diarylimines, vinyl ketones and simple amines. In the presence of a rhodium catalyst and Cu oxidant, four C-H and two N-H bonds are activated along with the formation of one new C-C and two new C-N bonds, leading to a series of isoindole derivatives in good to very high isolated yields.

Efficient Imine Formation by Oxidative Coupling at Low Temperature Catalyzed by High-Surface-Area Mesoporous CeO2 with Exceptional Redox Property

Wu, Shipeng,Wang, Yinghao,Cao, Qiue,Zhao, Qihua,Fang, Wenhao

supporting information, p. 3019 - 3028 (2020/12/11)

High-surface-area mesoporous CeO2 (hsmCeO2) was prepared by a facile organic-template-induced homogeneous precipitation process and showed excellent catalytic activity in imine synthesis in the absence of base from primary alcohols and amines in air atmosphere at low temperature. For comparison, ordinary CeO2 and hsmCeO2 after different thermal treatments were also investigated. XRD, N2 physisorption, UV-Raman, H2 temperature-programmed reduction, O2 temperature-programmed desorption, EPR spectroscopy, and X-ray photoelectron spectroscopy were used to unravel the structural and redox properties. The hsmCeO2 calcined at 400 °C shows the highest specific surface area (158 m2 g?1), the highest fraction of surface coordinatively unsaturated Ce3+ ions (18.2 %), and the highest concentration of reactive oxygen vacancies (2.4×1015 spins g?1). In the model reaction of oxidative coupling of benzyl alcohol and aniline, such an exceptional redox property of the hsmCeO2 catalyst can boost benzylideneaniline formation (2.75 and 5.55 mmol (Formula presented.) h?1 based on >99 % yield at 60 and 80 °C, respectively) in air with no base additives. It can also work effectively at a temperature of 30 °C and in gram-scale synthesis. These are among the best results for all benchmark ceria catalysts in the literature. Moreover, the hsmCeO2 catalyst shows a wide scope towards primary alcohols and amines with good to excellent yield of imines. The influence of reaction parameters, the reusability of the catalyst, and the reaction mechanism were investigated.

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