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CAS

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350610-39-8

Ethanone, 1-[(1R,2S)-2-hydroxy-2-methylcyclohexyl]-, rel- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 350610-39-8 Structure

  • Basic information

    1. Product Name: Ethanone, 1-[(1R,2S)-2-hydroxy-2-methylcyclohexyl]-, rel- (9CI)
    2. Synonyms: Ethanone, 1-[(1R,2S)-2-hydroxy-2-methylcyclohexyl]-, rel- (9CI)
    3. CAS NO:350610-39-8
    4. Molecular Formula: C9H16O2
    5. Molecular Weight: 156.22214
    6. EINECS: N/A
    7. Product Categories: ACETYLGROUP
    8. Mol File: 350610-39-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 244.3±33.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.020±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.73±0.40(Predicted)
    10. CAS DataBase Reference: Ethanone, 1-[(1R,2S)-2-hydroxy-2-methylcyclohexyl]-, rel- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Ethanone, 1-[(1R,2S)-2-hydroxy-2-methylcyclohexyl]-, rel- (9CI)(350610-39-8)
    12. EPA Substance Registry System: Ethanone, 1-[(1R,2S)-2-hydroxy-2-methylcyclohexyl]-, rel- (9CI)(350610-39-8)

  • 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: 350610-39-8(Hazardous Substances Data)

350610-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 350610-39-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,0,6,1 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 350610-39:
(8*3)+(7*5)+(6*0)+(5*6)+(4*1)+(3*0)+(2*3)+(1*9)=108
108 % 10 = 8
So 350610-39-8 is a valid CAS Registry Number.

350610-39-8Downstream Products

350610-39-8Relevant articles and documents

Stoichiometric and catalytic reductive aldol cyclizations of alkynediones induced by Stryker's reagent

Chiu, Pauline,Leung, Sze Kar

, p. 2308 - 2309 (2007/10/03)

Conjugate reduction of alkynones by stoichiometric [(Ph3P)CuH] 6 or catalytic [(Ph3P)CuH]6 and polymethylhydrosiloxane proceeds to cyclization by an aldol reaction with tethered ketones to generate β-hydroxyenon

Tandem conjugate reduction-aldol cyclization using stryker's reagent

Chiu, Pauline,Szeto, Chun-Pong,Geng, Zhe,Cheng, Kin-Fai

, p. 1901 - 1903 (2007/10/03)

(formula presentation) Conjugate reduction by Stryker's reagent to form copper enolates, followed by intramolecular aldol cyclization, successfully generated five- and six-membered carbocycles in one pot efficiently. This tandem reaction is generally dias

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