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Isoxazole, 5-chloro-4-methyl-3-phenyl-, is a chemical compound belonging to the isoxazole class, characterized by a five-membered heterocyclic ring containing one oxygen and one nitrogen atom. This specific compound features a 5-chloro substituent, a 4-methyl group, and a 3-phenyl group attached to the isoxazole ring. It is represented by the chemical formula C10H8ClNO and has a molecular weight of 189.63 g/mol. Isoxazole, 5-chloro-4-methyl-3-phenyl- is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The 5-chloro-4-methyl-3-phenyl-isoxazole exhibits potential applications in the development of new drugs and pesticides, making it an important intermediate in the chemical industry.

3356-90-9

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3356-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3356-90-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3356-90:
(6*3)+(5*3)+(4*5)+(3*6)+(2*9)+(1*0)=89
89 % 10 = 9
So 3356-90-9 is a valid CAS Registry Number.

3356-90-9SDS

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 5-chloro-4-methyl-3-phenyl-1,2-oxazole

1.2 Other means of identification

Product number -
Other names 5-Chlor-4-methyl-3-phenyl-isoxazol

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:3356-90-9 SDS

3356-90-9Relevant academic research and scientific papers

Complementing Pyridine-2,6-bis(oxazoline) with Cyclometalated N-Heterocyclic Carbene for Asymmetric Ruthenium Catalysis

Li, Long,Han, Feng,Nie, Xin,Hong, Yubiao,Ivlev, Sergei,Meggers, Eric

, p. 12392 - 12395 (2020/06/10)

A strategy for expanding the utility of chiral pyridine-2,6-bis(oxazoline) (pybox) ligands for asymmetric transition metal catalysis is introduced by adding a bidentate ligand to modulate the electronic properties and asymmetric induction. Specifically, a ruthenium(II) pybox fragment is combined with a cyclometalated N-heterocyclic carbene (NHC) ligand to generate catalysts for enantioselective transition metal nitrenoid chemistry, including ring contraction to chiral 2H-azirines (up to 97 % ee with 2000 TON) and enantioselective C(sp3)?H aminations (up to 97 % ee with 50 TON).

Asymmetric Synthesis of 2H-Azirines with a Tetrasubstituted Stereocenter by Enantioselective Ring Contraction of Isoxazoles

Okamoto, Kazuhiro,Nanya, Atsushi,Eguchi, Akira,Ohe, Kouichi

, p. 1039 - 1043 (2018/01/26)

Highly strained 2H-azirines with a tetrasubstituted stereocenter were synthesized by the enantioselective isomerization of isoxazoles with a chiral diene–rhodium catalyst system. The effect of ligands and the coordination behavior support the proposed cat

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