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CAS

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602-50-6

2-(diphenylmethyl)benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 602-50-6 Structure

  • Basic information

    1. Product Name: 2-(diphenylmethyl)benzoic acid
    2. Synonyms:
    3. CAS NO:602-50-6
    4. Molecular Formula: C20H16O2
    5. Molecular Weight: 288.3398
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 602-50-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 447.1°C at 760 mmHg
    3. Flash Point: 207.2°C
    4. Appearance: N/A
    5. Density: 1.175g/cm3
    6. Vapor Pressure: 8.9E-09mmHg at 25°C
    7. Refractive Index: 1.626
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(diphenylmethyl)benzoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(diphenylmethyl)benzoic acid(602-50-6)
    12. EPA Substance Registry System: 2-(diphenylmethyl)benzoic acid(602-50-6)

  • 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: 602-50-6(Hazardous Substances Data)

602-50-6 Usage

Structure

A benzoic acid molecule attached to a diphenylmethyl group

Pharmaceutical and medical applications

Used as an anti-inflammatory and analgesic drug

Inhibits production of inflammatory cytokines

May be effective in treating conditions such as arthritis and other inflammatory diseases

Sunscreen ingredient

Has potential due to its UV absorption properties

Check Digit Verification of cas no

The CAS Registry Mumber 602-50-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 602-50:
(5*6)+(4*0)+(3*2)+(2*5)+(1*0)=46
46 % 10 = 6
So 602-50-6 is a valid CAS Registry Number.

602-50-6Relevant articles and documents

Strategic Approach to the Metamorphosis of γ-Lactones to NH γ-Lactams via Reductive Cleavage and C-H Amidation

Jung, Hoi-Yun,Chang, Sukbok,Hong, Sungwoo

supporting information, p. 7099 - 7103 (2019/09/07)

A new approach has elaborated on the conversion of γ-lactones to the corresponding NH γ-lactams that can serve as γ-lactone bioisosteres. This approach consists of reductive C-O cleavage and an Ir-catalyzed C-H amidation, offering a powerful synthetic tool for accessing a wide range of valuable NH γ-lactam building blocks starting from γ-lactones. The synthetic utility was further demonstrated by the late-stage transformation of complex bioactive molecules and the asymmetric transformation.

Lithiierung in α-Stellung zum N-Atom von Triphenylacetamiden aus cyclischen sekundaeren Aminen. Umlagerung metallierter Triphenylacetamide unter 1,3-Verschiebung der Carbamoylgruppe

Wykypiel, Werner,Lohmann, Jean-Jaques,Seebach, Dieter

, p. 1337 - 1346 (2007/10/02)

The reagents 2 - generally available by lithiation of the triphenylacetamides 1 - react with non-enolizable carbonyl compounds and benzyl halide (s.Tables 1 and 2, and products 3).The limits of thermal stability of metalated triphenylacetamides above 0 de

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