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(2S,3S)-2,3-Dimethyl-2-(3-oxo-butyl)-cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 121843-01-4 Structure
  • Basic information

    1. Product Name: (2S,3S)-2,3-Dimethyl-2-(3-oxo-butyl)-cyclohexanone
    2. Synonyms: (2S,3S)-2,3-Dimethyl-2-(3-oxo-butyl)-cyclohexanone
    3. CAS NO:121843-01-4
    4. Molecular Formula:
    5. Molecular Weight: 196.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121843-01-4.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: (2S,3S)-2,3-Dimethyl-2-(3-oxo-butyl)-cyclohexanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3S)-2,3-Dimethyl-2-(3-oxo-butyl)-cyclohexanone(121843-01-4)
    11. EPA Substance Registry System: (2S,3S)-2,3-Dimethyl-2-(3-oxo-butyl)-cyclohexanone(121843-01-4)
  • 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: 121843-01-4(Hazardous Substances Data)

121843-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121843-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,8,4 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 121843-01:
(8*1)+(7*2)+(6*1)+(5*8)+(4*4)+(3*3)+(2*0)+(1*1)=94
94 % 10 = 4
So 121843-01-4 is a valid CAS Registry Number.

121843-01-4Downstream Products

121843-01-4Relevant articles and documents

Total synthesis of five natural eremophilane-type sesquiterpenoids

Meng, Zhe,Liu, Bo

, p. 957 - 962 (2018/02/19)

The first total syntheses of five natural eremophilane-type sesquiterpenoids were achieved in 4-12 steps via a common synthetic intermediate. The syntheses feature a double Michael addition, Robinson annulation, α-enolization of an unsaturated ketone, and

Efficient Trapping of Ketone Enolates with Acrylate and β-Sulfonylacrylate Thioesters, β-Sulfonyl-, β-sulfinyl- and β-Chloro-vinyl Ketones; Facile Preparation of a Hydrindanone, cis-Dimethyloctalone, and Unsaturated 1,5-Dicarbonyl Compounds

Dancer, Robert J.,Haynes, Richard K.,Laughlin, Wendy A.,Vonwiller, Simone C.

, p. 1375 - 1389 (2007/10/02)

Tandem conjugate addition-ring closure involving reaction of the lithium enolate arising from conjugate addition of lithiated (E)-but-2-enyldiphenylphosphine oxide to 2-methyl-cyclopent-2-enone with two moles of t-butylthioacrylate generates a hydrindanol

EPC Syntheses from Bicyclic Dioxanones: (-)-5-Epidehydrofukinone

Herradon, Bernardo

, p. 977 - 980 (2007/10/02)

(-)-5-Epidehydrofukinone ((-)-15) has been synthesized from (2S,4aS,5S,8aS)-4a,5-dimethyl-2-(tert-butyl)-perhydro-4H-1,3-benzodioxan-4-one (4a), a compound readily available by yeast reduction of ethyl 2-oxocyclohexanecarboxylate.

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