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875820-12-5

(2-NAPHTHYLOXY)(PHENYL)ACETIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 875820-12-5 Structure

  • Basic information

    1. Product Name: (2-NAPHTHYLOXY)(PHENYL)ACETIC ACID
    2. Synonyms: (2-NAPHTHYLOXY)(PHENYL)ACETIC ACID
    3. CAS NO:875820-12-5
    4. Molecular Formula: C18H14O3
    5. Molecular Weight: 278.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 875820-12-5.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-NAPHTHYLOXY)(PHENYL)ACETIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-NAPHTHYLOXY)(PHENYL)ACETIC ACID(875820-12-5)
    11. EPA Substance Registry System: (2-NAPHTHYLOXY)(PHENYL)ACETIC ACID(875820-12-5)

  • 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: 875820-12-5(Hazardous Substances Data)

875820-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 875820-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,5,8,2 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 875820-12:
(8*8)+(7*7)+(6*5)+(5*8)+(4*2)+(3*0)+(2*1)+(1*2)=195
195 % 10 = 5
So 875820-12-5 is a valid CAS Registry Number.

875820-12-5Upstream product

875820-12-5Downstream Products

875820-12-5Relevant articles and documents

CARBOXYLIC ACID DERIVATIVE AS AT2R RECEPTOR ANTAGONIST

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Paragraph 0093-0095, (2020/03/24)

The present invention relates to a compound shown in formula (II) or a pharmaceutically acceptable salt thereof and an application of the same in preparing a drug for treating a disease related to angiotensin II receptor type 2 (AT2R).(II)

Enantioselective palladium-catalyzed insertion of α-aryl-α- diazoacetates into the O-H bonds of phenols

Xie, Xiu-Lan,Zhu, Shou-Fei,Guo, Jun-Xia,Cai, Yan,Zhou, Qi-Lin

supporting information, p. 2978 - 2981 (2014/04/03)

A palladium-catalyzed asymmetric O-H insertion reaction was developed. Palladium complexes with chiral spiro bisoxazoline ligands promoted the insertion of α-aryl-α-diazoacetates into the O-H bond of phenols with high yield and excellent enantioselectivity under mild reaction conditions. This palladium-catalyzed asymmetric O-H insertion reaction provided an efficient and highly enantioselective method for the preparation of synthetically useful optically active α-aryl-α-aryloxyacetates.

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