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Phenol, 4-[[(4-hydroxyphenyl)imino]methyl]-2-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 27998-04-5 Structure
  • Basic information

    1. Product Name: Phenol, 4-[[(4-hydroxyphenyl)imino]methyl]-2-methoxy-
    2. Synonyms:
    3. CAS NO:27998-04-5
    4. Molecular Formula: C14H13NO3
    5. Molecular Weight: 243.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 27998-04-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Phenol, 4-[[(4-hydroxyphenyl)imino]methyl]-2-methoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenol, 4-[[(4-hydroxyphenyl)imino]methyl]-2-methoxy-(27998-04-5)
    11. EPA Substance Registry System: Phenol, 4-[[(4-hydroxyphenyl)imino]methyl]-2-methoxy-(27998-04-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 27998-04-5(Hazardous Substances Data)

27998-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27998-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,9 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27998-04:
(7*2)+(6*7)+(5*9)+(4*9)+(3*8)+(2*0)+(1*4)=165
165 % 10 = 5
So 27998-04-5 is a valid CAS Registry Number.

27998-04-5Relevant articles and documents

High-performance, command-degradable, antibacterial Schiff base epoxy thermosets: Synthesis and properties

Xu, Xiwei,Ma, Songqi,Wu, Jiahui,Yang, Jintao,Wang, Binbo,Wang, Sheng,Li, Qiong,Feng, Jie,You, Shusen,Zhu, Jin

, p. 15420 - 15431 (2019)

Two diepoxides containing a two-benzene-ring-conjugated Schiff base when cured with an aromatic diamine result in high-performance thermosets combining excellent controlled degradability, stability and antibacterial properties. Epoxy resins have been wide

Recyclable and Malleable Epoxy Thermoset Bearing Aromatic Imine Bonds

Zhao, Shou,Abu-Omar, Mahdi M.

, (2018/12/14)

A method for preparing reprocessable epoxy thermoset is presented. The process is composed of synthesis of a bisphenol monomer bridged by an imine bond, glycidylation of the bisphenol, and cross-linking with a hardener to form thermoset. The resulting epo

Recyclable and Malleable Epoxy Thermoset Bearing Aromatic Imine Bonds

Zhao, Shou,Abu-Omar, Mahdi M.

, p. 9816 - 9824 (2019/01/03)

A method for preparing reprocessable epoxy thermoset is presented. The process is composed of synthesis of a bisphenol monomer bridged by an imine bond, glycidylation of the bisphenol, and cross-linking with a hardener to form thermoset. The resulting epo

Synthesis of azomethines derived from cinnamaldehyde and vanillin: in vitro aetylcholinesterase inhibitory, antioxidant and insilico molecular docking studies

Chigurupati, Sridevi,Selvaraj, Manikandan,Mani, Vasudevan,Mohammad, Jahidul I.,Selvarajan, Kesavanarayanan K.,Akhtar, Shaikh S.,Marikannan, Maharajan,Raj, Suthakaran,Teh, Lay K.,Salleh, Mohd Z.

, p. 807 - 816 (2017/11/16)

In the present study, we report the synthesis of azomethines derived from cinnamaldehyde (C1–C3) and vanillin (V1–V3) using ethanol as a green solvent in the presence of triethyl amine. The synthesized compounds were characterized and investigated for the

Synthesis, structure-activity relationships and preliminary mechanism study of N-benzylideneaniline derivatives as potential TLR2 inhibitors

Cai, Shaoyi,Zhu, Gengzheng,Cen, Xiaohong,Bi, Jingjie,Zhang, Jingru,Tang, Xiaoshan,Chen, Kun,Cheng, Kui

, p. 2041 - 2050 (2018/03/13)

Toll-like receptor 2 (TLR2) can recognize pathogen-associated molecular patterns to defense against invading organisms and has been represents an attractive therapeutic target. Until today, none TLR2 small molecule antagonist have been developed in clinic

Spectral investigation of the activities of amino substituted bases

Ashraf, Muhammad Aqeel,Wajid, Abdul,Mahmood, Karamat,Maah, Mohd. Jamil,Yusoff, Ismail

experimental part, p. 363 - 372 (2012/04/04)

Three new series of biologically active amino substituted Schiff bases with general formula, R1N=CHR2. Here R1 = 2-amino-benzthiazole, 4-amino-salicylic acid and 4-aminophenol. R 2=4-chloro-benzaldehyde, 2-chloro-benzaldehyde, salicylaldehyde, vanillin and benzaldehyde were synthesized by the reaction of three different amino substituted compounds and substituted aldehydes in ethanol. Such compounds were characterized by different physico-chemical techniques like, melting point, elemental analysis, multinuclear nmr (1H, 13C). The free ligands and their metal complexes have been screened for their in vitro biological activities against bacteria, fungi and yeast. The metal complexes show more potent activities compared with Schiff base ligands.

Evaluation of antibacterial activity of some Schiff bases

Baluja, Shipra,Parikh, Jigna,Chanda, Sumitra,Vaishnani

experimental part, p. 1338 - 1342 (2010/08/05)

From 4-amino phenol, some Schiff bases were synthesized. By IR and NMR spectral data, the structural characterization of these synthesized compounds were done. The antibacterial activity of all these synthesized Schiff bases was studied against B. cereus-ATCC 11778, P. aero-ATCC 27853, E. coli-ATCC 25922, K pneu-NCIM 2719 and 5. aureus-ATCC 25923, by agar ditch method in dimethyl formamide and dimethyl sulfoxide. It is observed that antibacterial activity depends on the molecular structure of Schiff base, solvent used and bacterial strain under consideration. Out of two solvents studied, dimethyl formamide is proved to be best and salicylaldehyde as side chain to 4-amino phenol could be used as lead molecule in drug designing i.e. in inhibiting above bacterial strains.

Silica gel supported sodium hydrogen sulfate as an efficient and reusable heterogeneous catalyst for the synthesis of imines in solvent-free conditions under microwave irradiation

Gopalakrishnan, Mannathusamy,Sureshkumar, Purushothaman,Kanagarajan, Vijayakumar,Thanusu, Jeyaraman,Govindaraju, Ramalingam

, p. 299 - 303 (2007/10/03)

This synthesis of imines has been carried out efficiently by the condensation of carbonyl compounds with amines in the presence of silica gel supported sodium hydrogen sulfate (NaHSO4.SiO2) as a heterogeneous catalyst under microwave irradiation in solvent-free conditions. NaHSO4.SiO2 can be recovered and re-used up to ten times by simple washing with diethyl ether after each use and activated in an oven at 120°C for 1 h, thus rendering the process more economical.

Magnesium perchlorate as an efficient catalyst for the synthesis of imines and phenylhydrazones

Chakraborti, Asit K.,Bhagat, Srikant,Rudrawar, Santosh

, p. 7641 - 7644 (2007/10/03)

Magnesium perchlorate has been found to be an efficient catalyst for the synthesis of imines and phenylhydrazones by the reaction of carbonyl compounds with amines and phenylhydrazine in high yields at room temperatures and in short times. The condensation of less electrophilic carbonyl compounds with poorly nucleophilic amines affords the imines in excellent yields.

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