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455330-81-1

2-[2-(2-bromo-5-methoxy-phenyl)-ethyl]-3-nitromethyl-cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 455330-81-1 Structure

  • Basic information

    1. Product Name: 2-[2-(2-bromo-5-methoxy-phenyl)-ethyl]-3-nitromethyl-cyclohexanone
    2. Synonyms: 2-[2-(2-bromo-5-methoxy-phenyl)-ethyl]-3-nitromethyl-cyclohexanone
    3. CAS NO:455330-81-1
    4. Molecular Formula:
    5. Molecular Weight: 370.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 455330-81-1.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: 2-[2-(2-bromo-5-methoxy-phenyl)-ethyl]-3-nitromethyl-cyclohexanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[2-(2-bromo-5-methoxy-phenyl)-ethyl]-3-nitromethyl-cyclohexanone(455330-81-1)
    11. EPA Substance Registry System: 2-[2-(2-bromo-5-methoxy-phenyl)-ethyl]-3-nitromethyl-cyclohexanone(455330-81-1)

  • 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: 455330-81-1(Hazardous Substances Data)

455330-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 455330-81-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,5,3,3 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 455330-81:
(8*4)+(7*5)+(6*5)+(5*3)+(4*3)+(3*0)+(2*8)+(1*1)=141
141 % 10 = 1
So 455330-81-1 is a valid CAS Registry Number.

455330-81-1Relevant articles and documents

Palladium-catalyzed intramolecular α-arylation of aliphatic ketone, formyl, and nitro groups

Muratake, Hideaki,Natsume, Mitsutaka,Nakai, Hiroshi

, p. 11783 - 11803 (2007/10/03)

Intramolecular arylation of properly designed substrates bearing a ketone, formyl, or nitro terminating group was achieved by use of a PdCl 2(Ph3P)2-Cs2CO3 reaction system to form a variety of carbocyclic compounds. Arylation in ketone compounds afforded benzene-annulated bridged or spirocycloalkanone derivatives, depending on the structure of the cyclization precursors. Arylation in formyl compounds occurred at the α-position (α-arylation) or at the carbonyl carbon (carbonyl-arylation) depending on the structure of the cyclization precursors and on the reaction solvent. An α-arylated secondary nitro group was partially transformed to ketone in the manner of the Nef reaction, whereas a tertiary nitro group was partially eliminated to afford a styrene-type olefin. Graphical Abstract

Synthesis of a compound having the essential structural unit for the hetisine-type of aconite alkaloids

Muratake, Hideaki,Natsume, Mitsutaka

, p. 2913 - 2917 (2007/10/03)

A hexacyclic compound 1, which carries an almost full structure of the hetisine skeleton lacking only the six-membered ring with an exo methylene group, was synthesized by applying an acetal-ene reaction on 5 for the bond formation of C-14 and C-20 as wel

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