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CAS

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87137-50-6

Ethyl 5-(benzyloxy)-3-hydroxy-3-methylpentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 87137-50-6 Structure

  • Basic information

    1. Product Name: Ethyl 5-(benzyloxy)-3-hydroxy-3-methylpentanoate
    2. Synonyms:
    3. CAS NO:87137-50-6
    4. Molecular Formula:
    5. Molecular Weight: 266.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87137-50-6.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: Ethyl 5-(benzyloxy)-3-hydroxy-3-methylpentanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethyl 5-(benzyloxy)-3-hydroxy-3-methylpentanoate(87137-50-6)
    11. EPA Substance Registry System: Ethyl 5-(benzyloxy)-3-hydroxy-3-methylpentanoate(87137-50-6)

  • 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: 87137-50-6(Hazardous Substances Data)

87137-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87137-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,3 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87137-50:
(7*8)+(6*7)+(5*1)+(4*3)+(3*7)+(2*5)+(1*0)=146
146 % 10 = 6
So 87137-50-6 is a valid CAS Registry Number.

87137-50-6Downstream Products

87137-50-6Relevant articles and documents

Enantioselective Hydrolysis of 3-Hydroxy-3-methylalkanoic Acid Esters with Pig Liver Esterase

Wilson, William K.,Baca, Shawn B.,Barber, Yolanda J.,Scallen, Terence J.,Morrow, Cary J.

, p. 3960 - 3966 (1983)

Pig liver esterase has been shown to stereoselectively hydrolyze the R enantiomer of several chiral 3-hydroxy-3-methylalkanoic acid esters of the form RC(Me)(OH)CH2COOR', where R = Et, CH2=CHCH2, Me(CH2)5, (MeO)2CHCH2, and PhCH2OCH2CH2 and R'= Me or Et.The unhydrolyzed ester and the reesterified carboxylic acid were analyzed for enantiomeric purity by NMR using the chiral shift reagent Eu(hfc)3.For the compounds studied, the S enantiomers consistently showed greater induced shifts.Products of the resolution are potential intermediates in the preparation of compactin analogues having defined stereochemistry at carbon-3.These analogues will be useful in testing the hypothesis that the hypocholesterolemic activity of compactin and its analogues resides in their ability to mimic the binding of mevaldic acid coenzyme A hemithioacetal to HMG-CoA reductase but not be reduced to mevalonate.

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