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4-methyl-2-[(3-methylbenzylidene)amino]phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 315671-71-7 Structure
  • Basic information

    1. Product Name: 4-methyl-2-[(3-methylbenzylidene)amino]phenol
    2. Synonyms: 4-methyl-2-[(3-methylbenzylidene)amino]phenol
    3. CAS NO:315671-71-7
    4. Molecular Formula: C15H15NO
    5. Molecular Weight: 225.2857
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 315671-71-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-methyl-2-[(3-methylbenzylidene)amino]phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methyl-2-[(3-methylbenzylidene)amino]phenol(315671-71-7)
    11. EPA Substance Registry System: 4-methyl-2-[(3-methylbenzylidene)amino]phenol(315671-71-7)
  • 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: 315671-71-7(Hazardous Substances Data)

315671-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 315671-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,5,6,7 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 315671-71:
(8*3)+(7*1)+(6*5)+(5*6)+(4*7)+(3*1)+(2*7)+(1*1)=137
137 % 10 = 7
So 315671-71-7 is a valid CAS Registry Number.

315671-71-7Relevant articles and documents

Design, Synthesis, and Biological Activity of New N -(Phenylmethyl)-benzoxazol-2-thiones as Macrophage Migration Inhibitory Factor (MIF) Antagonists: Efficacies in Experimental Pulmonary Hypertension

Le Hiress, Morane,Akagah, Bernardin,Bernadat, Guillaume,Tu, Ly,Thuillet, Rapha?l,Huertas, Alice,Phan, Carole,Fadel, Elie,Simonneau, Gérald,Humbert, Marc,Jalce, Ga?l,Guignabert, Christophe

, p. 2725 - 2736 (2018/04/23)

Macrophage migration inhibitory factor (MIF) is a key pleiotropic mediator and a promising therapeutic target in cancer as well as in several inflammatory and cardiovascular diseases including pulmonary arterial hypertension (PAH). Here, a novel series of N-(phenylmethyl)-benzoxazol-2-thiones 5-32 designed to target the MIF tautomerase active site was synthesized and evaluated for its effects on cell survival. Investigation of structure-activity relationship (SAR) particularly at the 5-position of the benzoxazole core led to the identification of 31 that potently inhibits cell survival in DU-145 prostate cancer cells and pulmonary endothelial cells derived from patients with idiopathic PAH (iPAH-ECs), two cell lines for which survival is MIF-dependent. Molecular docking studies helped to interpret initial SAR related to MIF tautomerase inhibition and propose preferred binding mode for 31 within the MIF tautomerase active site. Interestingly, daily treatment with 31 started 2 weeks after a subcutaneous monocrotaline injection regressed established pulmonary hypertension in rats.

Synthesis of 2-substituted pyrimidines and benzoxazoles via a visible-light-driven organocatalytic aerobic oxidation: Enhancement of the reaction rate and selectivity by a base

Wang, Lin,Ma, Zhi-Gang,Wei, Xiao-Jing,Meng, Qing-Yuan,Yang, Deng-Tao,Du, Shao-Fu,Chen, Zi-Fei,Wu, Li-Zhu,Liu, Qiang

supporting information, p. 3752 - 3757 (2014/08/05)

An efficient visible-light-driven photocatalytic oxidation of various 2-substituted dihydropyrimidines and phenolic imines has been achieved using an organic photocatalyst eosin Y bis(tetrabutyl ammonium salt) (TBA-eosin Y) and inexpensive oxidant molecular oxygen. With the aid of a base, significantly enhanced photoinduced electron transfer from substrates dihydropyrimidines or phenolic imines to the excited state of TBA-eosin Y has enabled the aerobic oxidation to yield 2-(methylthio)pyrimidines or 2-arylbenzoxazoles selectively. This journal is the Partner Organisations 2014.

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