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5-methyl-4-(piperidin-1-ylmethyl)-2-(propan-2-yl)phenol is a complex organic compound with a molecular formula of C18H29NO. It features a phenol group, which is a hydroxyl group (-OH) attached to a benzene ring, with a methyl group (-CH3) at the 5th position and a propyl group (-C3H7) at the 2nd position. The piperidin-1-ylmethyl group is attached to the 4th position of the benzene ring, which is a piperidine ring (a cyclic amine with six members) with a methyl group attached to the nitrogen atom. 5-methyl-4-(piperidin-1-ylmethyl)-2-(propan-2-yl)phenol is known for its potential applications in pharmaceuticals and as a chemical intermediate, particularly in the synthesis of certain drugs and other organic compounds. Its structure and properties make it a versatile building block in organic synthesis, though it is important to note that specific applications and safety considerations should be evaluated based on the intended use and regulatory guidelines.

5408-16-2

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5408-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5408-16-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5408-16:
(6*5)+(5*4)+(4*0)+(3*8)+(2*1)+(1*6)=82
82 % 10 = 2
So 5408-16-2 is a valid CAS Registry Number.

5408-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-4-(piperidin-1-ylmethyl)-2-propan-2-ylphenol

1.2 Other means of identification

Product number -
Other names 1-<(4-Hydroxy-3-isopropyl-6-methyl-phenyl)-methyl>-piperidin

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:5408-16-2 SDS

5408-16-2Relevant academic research and scientific papers

Design, molecular docking, and antimicrobial assessment of newly synthesized phytochemical thymol Mannich base derivatives

Bishoyi, Ajit Kumar,Mahapatra, Monalisa,Padhy, Rabindra Nath,Paidesetty, Sudhir Kumar

, (2021/07/28)

Antibacterial resistance has been brewing for decades and has now surfaced into potential public health emergency, everywhere. Thus, newer potent drug candidates are needed urgently that would help overcoming antibiotic resistances in bacteria and fungi.

Carbonic anhydrase inhibition and cytotoxicity studies of Mannich base derivatives of thymol

Inci Gul, Halise,Yamali, Cem,Tugce Yasa, Asiye,Unluer, Elif,Sakagami, Hiroshi,Tanc, Muhammet,Supuran, Claudiu T.

, p. 1375 - 1380 (2016/10/09)

Mannich bases of thymol were synthesized. The aminomethylation reaction was realised in the ortho position of the phenol for compounds 2 (dipropylamine), 3 (benzylamine), and 4 (dibenzylamine) while it was from para position for 1 (dimethylamine), 5 (pipe

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