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CAS

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147029-77-4

4'-nitro-3-hydroxybenzophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 147029-77-4 Structure

  • Basic information

    1. Product Name: 4'-nitro-3-hydroxybenzophenone
    2. Synonyms: 4'-nitro-3-hydroxybenzophenone
    3. CAS NO:147029-77-4
    4. Molecular Formula:
    5. Molecular Weight: 243.219
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 147029-77-4.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: 4'-nitro-3-hydroxybenzophenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4'-nitro-3-hydroxybenzophenone(147029-77-4)
    11. EPA Substance Registry System: 4'-nitro-3-hydroxybenzophenone(147029-77-4)

  • 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: 147029-77-4(Hazardous Substances Data)

147029-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147029-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,0,2 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 147029-77:
(8*1)+(7*4)+(6*7)+(5*0)+(4*2)+(3*9)+(2*7)+(1*7)=134
134 % 10 = 4
So 147029-77-4 is a valid CAS Registry Number.

147029-77-4Relevant articles and documents

Total Synthesis of Termicalcicolanone A via Organocatalysis and Regioselective Claisen Rearrangement

Ito, Saki,Kitamura, Taiki,Arulmozhiraja, Sundaram,Manabe, Kei,Tokiwa, Hiroaki,Suzuki, Yumiko

, p. 2777 - 2781 (2019)

A total synthesis of an anticancer xanthone natural product termicalcicolanone A utilizing multiple nucleophilic aromatic substitutions and pericyclic reactions has been developed. The pyrano[3,2-b]xanthen-6-one scaffold was constructed via NHC-catalyzed

Glycosylated Derivatives of Benzophenone, Benzhydrol, and Benzhydril as Potential Venous Antithrombotic Agents

Bellamy, Francois,Horton, Derek,Millet, Jean,Picart, Francois,Samreth, Soth,Chazan, Jean Bernard

, p. 898 - 903 (2007/10/02)

A series of glycosylated derivatives of benzophenone, benzhydrol, and benzhydril has been synthesized and evaluated for potential activity as venous antithrombotic agents.Studies on structure-activity relationships revealed that compounds having an electr

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