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5-methyl-4-{[(E)-(4-methylphenyl)methylidene]amino}-2-(propan-2-yl)phenol is a complex organic compound characterized by its unique molecular structure. 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 compound also has an amino group (-NH2) connected to a benzylidene group, which is a carbonyl group (C=O) bonded to a benzene ring. The benzene ring in the benzylidene group is substituted with a methyl group at the 4th position, and the double bond in the benzylidene group is in the E configuration, indicating that the substituents are on opposite sides of the double bond. 5-methyl-4-{[(E)-(4-methylphenyl)methylidene]amino}-2-(propan-2-yl)phenol is likely to be found in the field of pharmaceuticals or as an intermediate in the synthesis of various organic compounds due to its complex structure and potential reactivity.

6325-49-1

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6325-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6325-49-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6325-49:
(6*6)+(5*3)+(4*2)+(3*5)+(2*4)+(1*9)=91
91 % 10 = 1
So 6325-49-1 is a valid CAS Registry Number.

6325-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-4-[(4-methylphenyl)methylideneamino]-2-propan-2-ylphenol

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:6325-49-1 SDS

6325-49-1Downstream Products

6325-49-1Relevant academic research and scientific papers

Synthesis and antioxidant activity of thymol and carvacrol based Schiff bases

Beena,Kumar, Deepak,Rawat, Diwan S.

supporting information, p. 641 - 645 (2013/03/13)

Thymol and carvacrol are well known antioxidants found in the extract of the plants of thyme species. The Schiff bases of 2-iso-propyl-5-methyl-phenol (thymol/1a), 2-tert-butyl-5-methyl-phenol (1b) and 5-iso-propyl-2-methyl-phenol (carvacrol/1c) exhibited much better antioxidant activity than thymol and carvacrol in DPPH assay. Ten compounds (4k, 4l, 4r, 5k, 5l, 5q, 5r, 6k, 6l and 6r) showed better or similar activity as compared to the reference compound ascorbic acid. Twenty-four most active compounds were also screened by ABTS method and showed 60-90% inhibition at 5 μg/mL concentration.

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