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Phenol, 2-[[[(2-hydroxy-5-methylphenyl)methyl]methylamino]methyl]-4,6-dimethyl- is a complex organic compound with the chemical formula C18H23NO. It is a derivative of phenol, characterized by the presence of a hydroxyl group (-OH) attached to a benzene ring. The molecule features a methyl group (-CH3) at the 5th position of the benzene ring and a methylamino group attached to the 2nd position. Additionally, it has two methyl groups at the 4th and 6th positions of the benzene ring. Phenol, 2-[[[(2-hydroxy-5-methylphenyl)methyl]methylamino]methyl]-4,6-dimethyl- is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity.

3534-24-5

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3534-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3534-24-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3534-24:
(6*3)+(5*5)+(4*3)+(3*4)+(2*2)+(1*4)=75
75 % 10 = 5
So 3534-24-5 is a valid CAS Registry Number.

3534-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-<2-Hydroxy-5-methyl-benzyl>-N-<2-hydroxy-3.5-dimethyl-benzyl>-methylamin

1.2 Other means of identification

Product number -
Other names N-(2-Hydroxy-5-methyl-benzyl)-N-(2-hydroxy-3.5-dimethyl-benzyl)-methylamin

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:3534-24-5 SDS

3534-24-5Relevant academic research and scientific papers

Polymerization of p-cresol, formaldehyde, and piperazine and structure of monofunctional benzoxazine-derived oligomers

Chutayothin, Papinporn,Ishida, Hatsuo

experimental part, p. 3897 - 3904 (2012/05/04)

By using a secondary amine, e g. piperazine, a Mannich base polymer, having similar structure to the traditional polybenzoxazine, is synthesized. Unlike all the reported polybenzoxazines that are colored, the white polymer shows good thermal property that is close to the degradation temperature of the polybenzoxazine derived from difunctional benzoxazine monomers. 31P NMR spectroscopy in combination with facile phosphorus derivatization and previous model compound studies are utilized to clarify the structures of piperazine-based systems as well as the main chain and end group of traditional polybenzoxazines.

Benzoxazine oligomers: Evidence for a helical structure from solid-state NMR spectroscopy and DFT-based dynamics and chemical shift calculations

Goward, Gillian R.,Sebastiani, Daniel,Schnell, Ingo,Spiess, Hans Wolfgang,Kim, Ho-Dong,Ishida, Hatsuo

, p. 5792 - 5800 (2007/10/03)

A combination of molecular modeling, DFT calculations, and advanced solid-state NMR experiments is used to elucidate the supramolecular structure of a series of benzoxazine oligomers. Intramolecular hydrogen bonds are characterized and identified as the d

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