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3-(1-propyl-2-nitroethyl)-2-cyclohexen-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134817-28-0 Structure
  • Basic information

    1. Product Name: 3-(1-propyl-2-nitroethyl)-2-cyclohexen-1-one
    2. Synonyms: 3-(1-propyl-2-nitroethyl)-2-cyclohexen-1-one
    3. CAS NO:134817-28-0
    4. Molecular Formula:
    5. Molecular Weight: 211.261
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134817-28-0.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-(1-propyl-2-nitroethyl)-2-cyclohexen-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(1-propyl-2-nitroethyl)-2-cyclohexen-1-one(134817-28-0)
    11. EPA Substance Registry System: 3-(1-propyl-2-nitroethyl)-2-cyclohexen-1-one(134817-28-0)
  • 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: 134817-28-0(Hazardous Substances Data)

134817-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134817-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,1 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 134817-28:
(8*1)+(7*3)+(6*4)+(5*8)+(4*1)+(3*7)+(2*2)+(1*8)=130
130 % 10 = 0
So 134817-28-0 is a valid CAS Registry Number.

134817-28-0Upstream product

134817-28-0Downstream Products

134817-28-0Relevant articles and documents

PREPARATION AND REACTIVITY OF FUNCIONALIZED ALKENYL-ZINC, -COPPER, AND -CHROMIUM ORGANOMETALLICS

Knochel, Paul,Rao, C. Janakiram

, p. 29 - 48 (1993)

β-Halogeno-α,β-unsaturated carbonyl derivatives were converted to the corresponding zinc organometallics 2a under mild conditions in THF (Zn dust, 25-45 deg C, 1-4h).These funcionalized alkenylzinc iodides react with a variety of alkenyl and aromatic iodides affording the desired coupling products in 40-97percent yield.The addition of a THF solution of CuCN*2LiCl to 2a affords the corresponding organocopper derivatives 2b which rect with electophiles, such as alkynyl and allylic halides, nitro olefins, enones, and chlorotrimethylstannane providing polyfuncional unsaturated carbonyl compounds in 71-95percent yield.The insertion of chromium (II) chloride to β-iodo and to some β-(p-tosyl)enones in DMF furnishes new funcionalized chromium (III) organometallics 2c which react with aldehydes providing γ-hydroxy unsaturated carbonyl derivatives in 40-91percent yield.The synthetic scope and the limitations of this methodology are discussed. Key words: funcionalized organozinc halides, alkenylchromium(III) compounds, copper-zinc organometallics.

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