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58240-93-0

METHYL CIS-3-HYDROXYMETHYLCYCLOPENTANE-1-CARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 58240-93-0 Structure

  • Basic information

    1. Product Name: METHYL CIS-3-HYDROXYMETHYLCYCLOPENTANE-1-CARBOXYLATE
    2. Synonyms: METHYL CIS-3-HYDROXYMETHYLCYCLOPENTANE-1-CARBOXYLATE;rel-methyl (1R,3S)-3-(hydroxymethyl)cyclopentane-1-carboxylate
    3. CAS NO:58240-93-0
    4. Molecular Formula: C8H14O3
    5. Molecular Weight: 158.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 58240-93-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 230°C at 760 mmHg
    3. Flash Point: 91.5°C
    4. Appearance: /
    5. Density: 1.091g/cm3
    6. Vapor Pressure: 0.0129mmHg at 25°C
    7. Refractive Index: 1.467
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: METHYL CIS-3-HYDROXYMETHYLCYCLOPENTANE-1-CARBOXYLATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: METHYL CIS-3-HYDROXYMETHYLCYCLOPENTANE-1-CARBOXYLATE(58240-93-0)
    12. EPA Substance Registry System: METHYL CIS-3-HYDROXYMETHYLCYCLOPENTANE-1-CARBOXYLATE(58240-93-0)

  • 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: 58240-93-0(Hazardous Substances Data)

58240-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58240-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,4 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58240-93:
(7*5)+(6*8)+(5*2)+(4*4)+(3*0)+(2*9)+(1*3)=130
130 % 10 = 0
So 58240-93-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O3/c1-11-8(10)7-3-2-6(4-7)5-9/h6-7,9H,2-5H2,1H3/t6-,7+/m0/s1

58240-93-0Relevant articles and documents

Pharmacophore-Based Design of Phenyl-[hydroxycyclohexyl] Cycloalkyl-Carboxamide Mitofusin Activators with Improved Neuronal Activity

Bernstein, Peter R.,Dang, Xiawei,Devanathan, Sriram,Dorn, Gerald W.,Franco, Antonietta,Fu, Lijun,Walters, Daniel,Williams, Sidney B.

, p. 12506 - 12524 (2021/09/11)

Mitochondrial fragmentation from defective fusion or unopposed fission contributes to many neurodegenerative diseases. Small molecule mitofusin activators reverse mitochondrial fragmentation in vitro, promising a novel therapeutic approach. The first-in-c

Substituted cyclopentane compounds useful as neuraminidase inhibitors

-

, (2008/06/13)

Compounds represented by formula (I), and pharmaceutically acceptacle salts thereof; and their method of preparation are provided. Compounds of the above formula are influenza virus neuraminidase inhibitors and can be used in treating patients infected with influenza virus.

Enzymes in organic synthesis. 33. Stereoselective pig liver esterase-catalyzed hydrolyses of meso cyclopentyl-, tetrahydrofuranyl-, and tetrahydrothiophenyl-1,3-diesters

Jones, J. Bryan,Hinks, R. Scott,Hultin, Philip G.

, p. 452 - 456 (2007/10/02)

Preparative-scale pig liver esterase-catalyzed hydrolyses of five-membered ring meso-1,3-diesters are enantiotopically selective.While pro-S enantiotopic selectivity is exhibited in each case, the absolute configuration sense of the hydrolysis in the cyclopentyl series is opposite to that of both the tetrahydrofuranyl and tetrahydrothiophenyl diesters.The enantiomeric excess levels induced are in the 34-46percent range.

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