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54112-42-4

2-Cyclopentene-1-methanol, 4-hydroxy-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54112-42-4 Structure

  • Basic information

    1. Product Name: 2-Cyclopentene-1-methanol, 4-hydroxy-, trans-
    2. Synonyms:
    3. CAS NO:54112-42-4
    4. Molecular Formula: C6H10O2
    5. Molecular Weight: 114.144
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54112-42-4.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: 2-Cyclopentene-1-methanol, 4-hydroxy-, trans-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Cyclopentene-1-methanol, 4-hydroxy-, trans-(54112-42-4)
    11. EPA Substance Registry System: 2-Cyclopentene-1-methanol, 4-hydroxy-, trans-(54112-42-4)

  • 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: 54112-42-4(Hazardous Substances Data)

54112-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54112-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,1 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54112-42:
(7*5)+(6*4)+(5*1)+(4*1)+(3*2)+(2*4)+(1*2)=84
84 % 10 = 4
So 54112-42-4 is a valid CAS Registry Number.

54112-42-4Relevant articles and documents

Deamination Reactions, 49. - Decomposition of 2-Oxa-5- and -6-norbornanediazonium Ions

Kirmse, Wolfgang,Mrotzeck, Uwe

, p. 485 - 492 (2007/10/02)

The reactivity of 2-oxa-6-norbornanediazonium ions (19, 20) conforms to that of the analogous brosylates (7, 11).Photolysis of the tosylhydrazone 17 in aqueous sodium hydroxide yields 2-oxa-exo-6-norbornanol (15) with no endo isomer 22.The deuterium incor

Cyclit-Reaktionen, II. Darstellung von Bausteinen zur Synthese carbocyclischer Furanose-Analoga

Paulsen, Hans,Maass, Uwe

, p. 346 - 358 (2007/10/02)

The four isomeric hydroxycyclopentenmethanols 6a to 9a can easily be made by allylhydroxylation of the epoxides 2 and 4 with phenyl selenide.In a second way the pair 8a and 9a has been synthesized from 11 via 15.As the preparation of 20 demonstrates, the functionalisation of 6a to 9a to carbocyclic furanoses is possible.The dicarboxylic diethyl esters 23 and 33 can be converted into models for carbocyclic ketofuranoses.

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