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1166398-65-7

1-hydroxymethyl-7-phenyl-2,1-benzisoxazol-3(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1166398-65-7 Structure

  • Basic information

    1. Product Name: 1-hydroxymethyl-7-phenyl-2,1-benzisoxazol-3(1H)-one
    2. Synonyms: 1-hydroxymethyl-7-phenyl-2,1-benzisoxazol-3(1H)-one
    3. CAS NO:1166398-65-7
    4. Molecular Formula:
    5. Molecular Weight: 241.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1166398-65-7.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: 1-hydroxymethyl-7-phenyl-2,1-benzisoxazol-3(1H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-hydroxymethyl-7-phenyl-2,1-benzisoxazol-3(1H)-one(1166398-65-7)
    11. EPA Substance Registry System: 1-hydroxymethyl-7-phenyl-2,1-benzisoxazol-3(1H)-one(1166398-65-7)

  • 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: 1166398-65-7(Hazardous Substances Data)

1166398-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1166398-65-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,6,3,9 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1166398-65:
(9*1)+(8*1)+(7*6)+(6*6)+(5*3)+(4*9)+(3*8)+(2*6)+(1*5)=187
187 % 10 = 7
So 1166398-65-7 is a valid CAS Registry Number.

1166398-65-7Downstream Products

1166398-65-7Relevant articles and documents

Synthesis of the lsoxazolo[4,3,2-de]phenanthridinone moiety of the parnafungins

Zhou, Quan,Snider, Barry B.

, p. 2936 - 2939 (2009)

A practical route to the labile tetracyclic lsoxazolo[4,3,2-de] phenanthrldlnone moiety of the antifungal parnafunglns has been developed. Zinc reduction of a methyl 2′-hydroxymethyl-2-nltro-3-blphenylcarboxylate, which was prepared by a Suzuki coupling,

Synthesis of hexacyclic parnafungin A and C models

Zhou, Quan,Snider, Barry B.

experimental part, p. 8224 - 8233 (2011/02/23)

A convergent, practical route to unstable hexacyclic parnafungin A and C models has been developed. Two iodoxanthones were prepared in four or five steps (33-50% overall yield). Suzuki-Miyaura coupling of the iodoxanthones with excess readily available 3-

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