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CAS

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129686-06-2

3-(propargyloxy)benzyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 129686-06-2 Structure

  • Basic information

    1. Product Name: 3-(propargyloxy)benzyl acetate
    2. Synonyms: 3-(propargyloxy)benzyl acetate
    3. CAS NO:129686-06-2
    4. Molecular Formula:
    5. Molecular Weight: 204.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129686-06-2.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: 3-(propargyloxy)benzyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(propargyloxy)benzyl acetate(129686-06-2)
    11. EPA Substance Registry System: 3-(propargyloxy)benzyl acetate(129686-06-2)

  • 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: 129686-06-2(Hazardous Substances Data)

129686-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129686-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,6,8 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129686-06:
(8*1)+(7*2)+(6*9)+(5*6)+(4*8)+(3*6)+(2*0)+(1*6)=162
162 % 10 = 2
So 129686-06-2 is a valid CAS Registry Number.

129686-06-2Relevant articles and documents

Preparation of carboranyl porphyrins for boron neutron capture therapy

Miura, Michiko,Gabel, Detlef,Oenbrink, Georg,Fairchild, Ralph G.

, p. 2247 - 2250 (1990)

The preparation of two structurally different boronated porphyrins is described for use in Boron Neutron Capture Therapy. One is a derivative of a natural porphyrin and the other is a derivative of tetraphenylporphyrin.

PROCESS FOR THE PREPARATION OF A SUBSTITUTED PORPHYRIN

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Page/Page column 20-21, (2010/11/08)

Processes are disclosed for the preparation of a compound having the formula: (I) and intermediate compounds wherein M is a single-photon-emission tomography imageable radiometal and/or a paramagnetic metal, R is hydrogen or a halogen provided that at least one R is halogen and Y is selected from ortho, meta or para O(CH2)nC2HB9H10 or O(CH2)nC2HB 10H10 wherein n is 0 or an integer from 1 to 20 and O(CH2)nC2HB9H10 is nido ortho-, meta- or para- carborane and O(CH2)nC2HB10H10 is ortho-, meta- or para-carborane.

DNA binding compounds. VII synthesis, characterization and DNA binding capacity of 1,2-dicarba-closo-dodecaborane bibenzimidazoles related to the DNA minor groove binder Hoechst 33258

Bateman, Stuart A.,Kelly, David P.,Martin, Roger F.,White, Jonathan M.

, p. 291 - 301 (2007/10/03)

A series of bibenzimidazole derivatives based on the known DNA minor groove binder Hoechst 33258 have been prepared to include a 1,2-dicarba-closo-dodecaborane cage for potential use in boron neutron capture therapy (BNCT). The carborane derivatives (5)-(7) were chosen to reduce the steric inhibition of minor groove DNA binding displayed by the previously prepared carborane ligand (4). The synthesis and preliminary DNA binding studies of these bibenzimidazole derivatives are presented herein.

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