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1335113-62-6

N-(3-bromopyridin-2-yl)-N-methyl-2-oxo-2-phenylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1335113-62-6 Structure

  • Basic information

    1. Product Name: N-(3-bromopyridin-2-yl)-N-methyl-2-oxo-2-phenylacetamide
    2. Synonyms: N-(3-bromopyridin-2-yl)-N-methyl-2-oxo-2-phenylacetamide
    3. CAS NO:1335113-62-6
    4. Molecular Formula:
    5. Molecular Weight: 319.158
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1335113-62-6.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-(3-bromopyridin-2-yl)-N-methyl-2-oxo-2-phenylacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(3-bromopyridin-2-yl)-N-methyl-2-oxo-2-phenylacetamide(1335113-62-6)
    11. EPA Substance Registry System: N-(3-bromopyridin-2-yl)-N-methyl-2-oxo-2-phenylacetamide(1335113-62-6)

  • 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: 1335113-62-6(Hazardous Substances Data)

1335113-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1335113-62-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,5,1,1 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1335113-62:
(9*1)+(8*3)+(7*3)+(6*5)+(5*1)+(4*1)+(3*3)+(2*6)+(1*2)=116
116 % 10 = 6
So 1335113-62-6 is a valid CAS Registry Number.

1335113-62-6Relevant articles and documents

Reductive cyclization of halo-ketones to form 3-hydroxy-2-oxindoles via palladium catalyzed hydrogenation: a hydrogen-mediated Grignard addition

Shin, Inji,Ramgren, Stephen D.,Krische, Michael J.

, p. 5776 - 5780 (2015/08/03)

Abstract The reductive cyclization of N-oxoacyl ortho-bromoanilides to form 3-hydroxy-2-oxindoles under the conditions of palladium catalyzed hydrogenation is described. This work may be viewed as a prelude to intermolecular hydrogen-mediated Grignard-typ

The preparation of 2H-1,4-benzoxazin-3-(4H)-ones via palladium-catalyzed intramolecular C-O bond formation

Ylijoki, Kai E. O.,Kuendig, E. Peter

supporting information; experimental part, p. 10608 - 10610 (2011/11/05)

Pd/PtBu3-catalyzed intramolecular C-O bond formation has been used to access aryl- and alkyl-substituted benzoxazinones.

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