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2-methoxy-5-methyl-N-[4-(methylsulfanyl)benzyl]aniline is a complex organic compound with the molecular formula C16H19NOS. It is a derivative of aniline, featuring a 2-methoxy group, a 5-methyl group, and a 4-(methylsulfanyl)benzyl group attached to the nitrogen atom. 2-methoxy-5-methyl-N-[4-(methylsulfanyl)benzyl]aniline is characterized by its aromatic structure and the presence of a sulfur atom in the form of a methyl sulfide group, which contributes to its unique chemical properties. It is likely to be used in the synthesis of variouss pharmaceutical, agrochemicals, or other specialty chemicals due to its diverse functional groups and potential reactivity.

5564-45-4

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5564-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5564-45-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,6 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5564-45:
(6*5)+(5*5)+(4*6)+(3*4)+(2*4)+(1*5)=104
104 % 10 = 4
So 5564-45-4 is a valid CAS Registry Number.

5564-45-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-phenyl-4,5,6,7-tetrahydroindazol-3-yl)acetic acid

1.2 Other means of identification

Product number -
Other names Z-Ser-Phe-O-benzyl

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:5564-45-4 SDS

5564-45-4Downstream Products

5564-45-4Relevant academic research and scientific papers

The small peptide-catalyzed direct asymmetric aldol reaction in water

Dziedzic, Pawel,Zou, Weibiao,Hafren, Jonas,Cordova, Armando

, p. 38 - 40 (2007/10/03)

The asymmetric aldol reaction is a powerful method for forming carbon-carbon bonds. Small peptides with a primary amine as the catalytic residue catalyze asymmetric aqueous aldol reactions between unmodified ketones and aldehydes to furnish the corresponding aldol products with high ees. The high momodularity of the small peptides should enable the construction of several novel catalysts by combinatorial techniques for the aqueous asymmetric aldol reaction. The remarkably high difference in stereoselectivity between the peptide bond-formation was an important step towards the evaluation of asymmetric catalysis and homochilarity.

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