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CAS

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54550-26-4

2-Propanone, 1-[(2-nitrobenzoyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54550-26-4 Structure

  • Basic information

    1. Product Name: 2-Propanone, 1-[(2-nitrobenzoyl)oxy]-
    2. Synonyms:
    3. CAS NO:54550-26-4
    4. Molecular Formula: C10H9NO5
    5. Molecular Weight: 223.185
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54550-26-4.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: 2-Propanone, 1-[(2-nitrobenzoyl)oxy]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Propanone, 1-[(2-nitrobenzoyl)oxy]-(54550-26-4)
    11. EPA Substance Registry System: 2-Propanone, 1-[(2-nitrobenzoyl)oxy]-(54550-26-4)

  • 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: 54550-26-4(Hazardous Substances Data)

54550-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54550-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,5 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54550-26:
(7*5)+(6*4)+(5*5)+(4*5)+(3*0)+(2*2)+(1*6)=114
114 % 10 = 4
So 54550-26-4 is a valid CAS Registry Number.

54550-26-4Downstream Products

54550-26-4Relevant articles and documents

Oxidative C-H Acyloxylation of Acetone with Carboxylic Acids under Iodine Catalysis

Zhou, Xiao-Yu,Chen, Xia

supporting information, p. 1654 - 1662 (2021/01/21)

Iodine-catalyzed oxidative C(sp 3)-H acyloxylation of acetone with carboxylic acids has been developed. The method employs iodide as catalyst and sodium chlorite as oxidant. Substituted benzoic acids, naphthoic acids and heteroaromatic carboxyl

Facile oxidative hydrolysis of acetals to esters using hypervalent iodine(III)/LiBr combination in water

Panchan, Waraporn,Chiampanichayakul, Supanimit,Snyder, Deanna L.,Yodbuntung, Siriporn,Pohmakotr, Manat,Reutrakul, Vichai,Jaipetch, Thaworn,Kuhakarn, Chutima

scheme or table, p. 2732 - 2735 (2010/05/17)

The combination of (diacetoxy)iodobenzene (PhI(OAc)2, DIB) and lithium bromide (LiBr) efficiently oxidized cyclic and acyclic acetals to the corresponding hydroxyalkyl carboxylic esters and simple esters in good to excellent yields. The merits of this reaction are that it employs commercially available and non-explosive hypervalent iodine(III) reagent, water as the solvent, a short reaction time, and mild reaction conditions.

Synthesis of 2-Substituted 1H-Benzoxazepin-5-ones

Sicker, Dieter

, p. 336 - 344 (2007/10/02)

An approach to the hitherto unknown class of 1H-benz>e>oxazepin-5-ones is given based on reduction and cyclization of appropriate acyclic ortho-nitro compounds as starting material.Thus, some 2-substituted derivatives (3a-i) were synthesized by catal

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