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1363440-02-1

N-(1-(4-iodophenyl)propan-2-yl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1363440-02-1 Structure

  • Basic information

    1. Product Name: N-(1-(4-iodophenyl)propan-2-yl)acetamide
    2. Synonyms: N-(1-(4-iodophenyl)propan-2-yl)acetamide
    3. CAS NO:1363440-02-1
    4. Molecular Formula:
    5. Molecular Weight: 289.116
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1363440-02-1.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: N-(1-(4-iodophenyl)propan-2-yl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1-(4-iodophenyl)propan-2-yl)acetamide(1363440-02-1)
    11. EPA Substance Registry System: N-(1-(4-iodophenyl)propan-2-yl)acetamide(1363440-02-1)

  • 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: 1363440-02-1(Hazardous Substances Data)

1363440-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1363440-02-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,4,4 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1363440-02:
(9*1)+(8*3)+(7*6)+(6*3)+(5*4)+(4*4)+(3*0)+(2*0)+(1*2)=131
131 % 10 = 1
So 1363440-02-1 is a valid CAS Registry Number.

1363440-02-1Relevant articles and documents

A unified photoredox-catalysis strategy for C(sp3)-H hydroxylation and amidation using hypervalent iodine

Li, Guo-Xing,Morales-Rivera, Cristian A.,Gao, Fang,Wang, Yaxin,He, Gang,Liu, Peng,Chen, Gong

, p. 7180 - 7185 (2017)

We report a unified photoredox-catalysis strategy for both hydroxylation and amidation of tertiary and benzylic C-H bonds. Use of hydroxyl perfluorobenziodoxole (PFBl-OH) oxidant is critical for efficient tertiary C-H functionalization, likely due to the enhanced electrophilicity of the benziodoxole radical. Benzylic methylene C-H bonds can be hydroxylated or amidated using unmodified hydroxyl benziodoxole oxidant Bl-OH under similar conditions. An ionic mechanism involving nucleophilic trapping of a carbocation intermediate by H2O or CH3CN cosolvent is presented.

NEW AZIRIDINE COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND THEIR USE AS ACETYL-COA CARBOXYLASE INHIBITORS

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Page/Page column 73, (2013/07/05)

The invention relates to new azetidine derivatives of the formula (I) wherein Ar1, Ar2, X, R, T and L are as defined in the description, to their use as medicaments, to methods for their therapeutic use and to pharmaceutical compositions containing them.

AZETIDINE DERIVATIVES

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Paragraph 0424; 0425; 0426; 0427; 0428, (2013/06/28)

Azetidine derivatives of which the following is exemplary and their use in the treatment of obesity, diabetes or dyslipidemia.

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