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109877-38-5

2-aMino-3-phenylphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 109877-38-5 Structure

  • Basic information

    1. Product Name: 2-aMino-3-phenylphenol
    2. Synonyms: 2-aMino-3-phenylphenol
    3. CAS NO:109877-38-5
    4. Molecular Formula: C12H11NO
    5. Molecular Weight: 185.22184
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 109877-38-5.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: 2-aMino-3-phenylphenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-aMino-3-phenylphenol(109877-38-5)
    11. EPA Substance Registry System: 2-aMino-3-phenylphenol(109877-38-5)

  • 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: 109877-38-5(Hazardous Substances Data)

109877-38-5 Usage

Class of compound

Phenols

Common uses

Production of dyes and pigments, synthesis of pharmaceuticals and organic materials

Potential properties

Antioxidant, anti-inflammatory

Physical characteristics

White to light beige color, solid at room temperature

Safety precautions

Toxic if swallowed or inhaled, can cause skin and eye irritation

Check Digit Verification of cas no

The CAS Registry Mumber 109877-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,8,7 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 109877-38:
(8*1)+(7*0)+(6*9)+(5*8)+(4*7)+(3*7)+(2*3)+(1*8)=165
165 % 10 = 5
So 109877-38-5 is a valid CAS Registry Number.

109877-38-5Relevant articles and documents

Access to C4-arylated benzoxazoles from 2-amidophenol through C-H activation

Panda, Niranjan,Pradhan, Priyanka,Sahoo, Kanchanbala

, p. 1820 - 1832 (2020/03/17)

A Pd-catalyzed aerobic approach to access C4-aryl benzoxazoles by tandem C-H ortho-arylation and acid-mediated annulation of 2-amidophenol has been presented. The directing potential of the -NHCOR group over the -OH group was exploited for selective arylation adjacent to the amide group. Deuterium labeling experiments suggest that palladation predominantly occurs adjacent to the -NHCOR group and is the key step during benzoxazole formation. One-pot hydrolysis of the resulting C4-arylated benzoxazole was also accomplished to access structurally challenging 3-aryl aminophenols for further applications.

Design, synthesis and structure-activity relationships of novel benzoxazolone derivatives as 18 kDa translocator protein (TSPO) ligands

Fukaya, Takayuki,Kodo, Toru,Ishiyama, Takeo,Kakuyama, Hiroyoshi,Nishikawa, Hiroyuki,Baba, Satoko,Masumoto, Shuji

, p. 5568 - 5582 (2012/10/29)

Selective 18 kDa translocator protein (TSPO) ligands are expected to be therapeutic agents with a wide spectrum of action on psychiatric disorders and fewer side effects. We designed novel benzoxazolone derivatives and examined the structure-activity rela

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