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Benzoic acid, 3-(benzoyloxy)-2-hydroxy-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 221684-52-2 Structure
  • Basic information

    1. Product Name: Benzoic acid, 3-(benzoyloxy)-2-hydroxy-, methyl ester
    2. Synonyms:
    3. CAS NO:221684-52-2
    4. Molecular Formula: C15H12O5
    5. Molecular Weight: 272.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 221684-52-2.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: Benzoic acid, 3-(benzoyloxy)-2-hydroxy-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 3-(benzoyloxy)-2-hydroxy-, methyl ester(221684-52-2)
    11. EPA Substance Registry System: Benzoic acid, 3-(benzoyloxy)-2-hydroxy-, methyl ester(221684-52-2)
  • 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: 221684-52-2(Hazardous Substances Data)

221684-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 221684-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,6,8 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 221684-52:
(8*2)+(7*2)+(6*1)+(5*6)+(4*8)+(3*4)+(2*5)+(1*2)=122
122 % 10 = 2
So 221684-52-2 is a valid CAS Registry Number.

221684-52-2Relevant articles and documents

ANAPLASTIC LYMPHOMA KINASE MODULATORS AND METHODS OF USE

-

Page/Page column 157, (2008/06/13)

The present invention comprises compounds and pharmaceutical compositions comprising the compounds that are inhibitors of ALK. The invention also comprises methods of using the compounds and compositions to treat diseases mediated by ALK, including diseases such as cancer, immunological disorders, cardiovascular diseases, and other degenerative disorders.

Dimerization of o-hydroxycyclohexadienones related to calicheamicinone: S(N)2 displacement of the 12α-hydroxyl group

Churcher, Ian,Hallett, David,Magnus, Philip

, p. 1597 - 1606 (2007/10/03)

Deprotection of the readily available bicyclo[7,3,1]enediyne alcohol 14 resulted in dimerization to give 18. Replacement of the 12α-hydroxyl group with a p-methoxyanilino group proceeded with overall retention to give 23 which also produced a dimer on attempted deprotection.

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