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141029-31-4

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141029-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141029-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,2 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 141029-31:
(8*1)+(7*4)+(6*1)+(5*0)+(4*2)+(3*9)+(2*3)+(1*1)=84
84 % 10 = 4
So 141029-31-4 is a valid CAS Registry Number.

141029-31-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (H51045)  N-(1-Naphthyl)-N-phenylmethacrylamide, 98%   

  • 141029-31-4

  • 250mg

  • 694.0CNY

  • Detail
  • Alfa Aesar

  • (H51045)  N-(1-Naphthyl)-N-phenylmethacrylamide, 98%   

  • 141029-31-4

  • 1g

  • 2019.0CNY

  • Detail
  • Aldrich

  • (565091)  N-(1-Naphthyl)-N-phenylmethacrylamide  98%

  • 141029-31-4

  • 565091-100MG

  • 720.72CNY

  • Detail

141029-31-4SDS

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 2-methyl-N-naphthalen-1-yl-N-phenylprop-2-enamide

1.2 Other means of identification

Product number -
Other names N-(1-Naphthyl)-N-phenylmethacrylamide

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:141029-31-4 SDS

141029-31-4Downstream Products

141029-31-4Relevant articles and documents

Photoredox Cyclization of N-Arylacrylamides for Synthesis of Dihydroquinolinones

Liu, Zhaosheng,Zhong, Shuai,Ji, Xiaochen,Deng, Guo-Jun,Huang, Huawen

, p. 349 - 353 (2021/12/27)

Metal- and additive-free photoredox cyclization of N-arylacrylamides is herein reported that provides a concise access to the formation of dihydroquinolinones. In this protocol, sustainable visible light was used as the energy source, and the organic light-emitting molecule 4CzIPN served as the efficient photocatalyst. This reaction system features exclusive 6-endo-trig cyclization selectivity with a generally good yield of a range of functionalized dihydroquinolinones and dihydrobenzoquinolinones. Mechanistical studies reveal the feasibility of both 1,3-H shift and intersystem crossing of the diradical intermediate.

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