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5-methyl-2-(propan-2-yl)-4-({(E)-[4-(propan-2-yl)phenyl]methylidene}amino)phenol is a complex organic compound characterized by its 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 a unique side chain that includes a (E)-[4-(propan-2-yl)phenyl]methylidene group, which is a double-bonded phenyl ring with a propyl group at the 4th position, attached to an amino group. This structure gives the compound its distinct chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research.

7251-23-2

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7251-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7251-23-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7251-23:
(6*7)+(5*2)+(4*5)+(3*1)+(2*2)+(1*3)=82
82 % 10 = 2
So 7251-23-2 is a valid CAS Registry Number.

7251-23-2SDS

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-2-propan-2-yl-4-[(4-propan-2-ylphenyl)methylideneamino]phenol

1.2 Other means of identification

Product number -
Other names 4-Cuminalamino-thymol

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:7251-23-2 SDS

7251-23-2Downstream Products

7251-23-2Relevant 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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