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1298063-71-4

(1R,2S,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1298063-71-4 Structure

  • Basic information

    1. Product Name: (1R,2S,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol
    2. Synonyms: (1R,2S,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol
    3. CAS NO:1298063-71-4
    4. Molecular Formula:
    5. Molecular Weight: 168.236
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1298063-71-4.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: (1R,2S,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,2S,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol(1298063-71-4)
    11. EPA Substance Registry System: (1R,2S,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol(1298063-71-4)

  • 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: 1298063-71-4(Hazardous Substances Data)

1298063-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1298063-71-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,8,0,6 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1298063-71:
(9*1)+(8*2)+(7*9)+(6*8)+(5*0)+(4*6)+(3*3)+(2*7)+(1*1)=184
184 % 10 = 4
So 1298063-71-4 is a valid CAS Registry Number.

1298063-71-4Downstream Products

1298063-71-4Relevant articles and documents

Highly potent activity of (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3- ene-1,2-diol in animal models of parkinson's disease

Ardashov, Oleg V.,Pavlova, Alla V.,Il'ina, Irina V.,Morozova, Ekaterina A.,Korchagina, Dina V.,Karpova, Elena V.,Volcho, Konstantin P.,Tolstikova, Tat'yana G.,Salakhutdinov, Nariman F.

experimental part, p. 3866 - 3874 (2011/08/07)

(1R,2R,6S)-3-Methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol 1 possesses potent antiparkinsonian activity in both MPTP and haloperidol animal models. The use of compound 1 resulted in nearly full recovery of the locomotor and exploratory activities and was as effective as the comparator agent (levodopa). All eight stereoisomers of compound 1 have been synthesized and the influence of the absolute configuration on the antiparkinsonian activity of compound 1 was shown.

Selective deoxygenation of allylic alcohol: Stereocontrolled synthesis of lavandulol

Kim, Hee Jin,Su, Liang,Jung, Heejung,Koo, Sangho

supporting information; experimental part, p. 2682 - 2685 (2011/06/26)

Selective deoxygenation of allylic alcohol can be successfully carried out by the formation of alkoxyalkyl ether (EE or MOM), followed by Pd(dppe)Cl 2-catalyzed reduction with LiBHEt3. (+)-S-Lavandulol has been efficiently synthesized by the application of this protocol to the diol derived from the Pb(OAc)4-promoted oxidative ring-opening of (-)-R-carvone. This deoxygenation method is general and selective for allylic alcohols.

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