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49647-20-3

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49647-20-3 Usage

Uses

4-Acetylphenyl isocyanate may be used for the preparation of isocyanate-treated graphene oxide (iGO). It may be used for the following syntheses:(4S,5R)-2-oxo-4-(4-phenyl-piperazin-1-ylmethyl)-oxazolidin-5-ylmethyl (4-acetyl-phenyl)-carbamate (4S,5R)-2-oxo-4-(4-phenyl-piperazin-1-ylmethyl)-oxazolidin-5-ylmethyl (4-acetyl-phenyl)-carbamate2-oxo-4-(4-phenyl-piperazin-1-ylmethyl)-oxazolidin-5-ylmethyl phenyl acetate2-oxo-4-(4-phenyl-piperazin-1-ylmethyl)-oxazolidin-5-ylmethyl (4-acetyl-phenyl)-carbamate

General Description

4-Acetylphenyl isocyanate is a reactive isocyanate and had one carbamate unit for every 7.6 graphene carbons.

Check Digit Verification of cas no

The CAS Registry Mumber 49647-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,4 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 49647-20:
(7*4)+(6*9)+(5*6)+(4*4)+(3*7)+(2*2)+(1*0)=153
153 % 10 = 3
So 49647-20-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO2/c1-7(12)8-2-4-9(5-3-8)10-6-11/h2-5H,1H3

49647-20-3 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L09665)  4-Acetylphenyl isocyanate, 97%   

  • 49647-20-3

  • 1g

  • 180.0CNY

  • Detail
  • Alfa Aesar

  • (L09665)  4-Acetylphenyl isocyanate, 97%   

  • 49647-20-3

  • 5g

  • 575.0CNY

  • Detail
  • Alfa Aesar

  • (L09665)  4-Acetylphenyl isocyanate, 97%   

  • 49647-20-3

  • 25g

  • 2478.0CNY

  • Detail
  • Aldrich

  • (439932)  4-Acetylphenylisocyanate  97%

  • 49647-20-3

  • 439932-1G

  • 326.43CNY

  • Detail
  • Aldrich

  • (439932)  4-Acetylphenylisocyanate  97%

  • 49647-20-3

  • 439932-10G

  • 1,595.88CNY

  • Detail

49647-20-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Acetylphenyl Isocyanate

1.2 Other means of identification

Product number -
Other names 4-Acetylphenyl isocyanate

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:49647-20-3 SDS

49647-20-3Relevant articles and documents

Design, synthesis, and antitumor activity of novel sorafenib derivatives

Chen, Dan-Ping,Fan, Si-Li,Hou, Mi,Li, Xiao-Qin,Li, Zhu-Rui,Ouyang, Gui-Ping,Shao, Li-Hui,Wang, Zhen-Chao,Zou, Ya-Yu

, (2022/01/26)

New series of 18 compounds were synthesized using sorafenib derivatives as parent structure and p-aminoacetophenone as raw materials. The structures of the newly synthesized compounds were confirmed on the basis of 1H, 13C NMR and HR

Synthesis and nematicidal activity of piperazinedione derivatives based on the natural product Barettin

Sun, Haiyang,Li, Hui,Wang, Jiayi,Song, Gonghua

, p. 977 - 980 (2017/11/16)

Nematodes are serious constraints of crop production worldwide. However, the traditional nematicides suffer from the side-effects, including environmental and human toxicity. Herein, more than 70 novel piperazinedione derivatives based on the natural product Barettin were synthesized and evaluated against the root-knot nematode Meloidogyne incognita (M. incognita). While most of synthesized compounds exhibited certain nematicidal activity at high concentration, the best one showed a nematicidal activity of 75% at 2.4 μmol/L.

Palladium-catalyzed synthesis of N-aryl carbamates

Vinogradova, Ekaterina V.,Park, Nathaniel H.,Fors, Brett P.,Buchwald, Stephen L.

supporting information, p. 1394 - 1397 (2013/04/24)

An efficient synthesis of aryl carbamates was achieved by introducing alcohols into the reaction of palladium-catalyzed cross-coupling of ArX (X = Cl, OTf) with sodium cyanate. The use of aryl triflates as electrophilic components in this transformation a

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