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251922-48-2

4-(Oxetan-3-yl)butan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 251922-48-2 Structure

  • Basic information

    1. Product Name: 4-(Oxetan-3-yl)butan-1-ol
    2. Synonyms: 4-(Oxetan-3-yl)butan-1-ol;3-Oxetanebutanol
    3. CAS NO:251922-48-2
    4. Molecular Formula: C7H14O2
    5. Molecular Weight: 130.18486
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 251922-48-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 226℃
    3. Flash Point: 95℃
    4. Appearance: /
    5. Density: 1.000
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(Oxetan-3-yl)butan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(Oxetan-3-yl)butan-1-ol(251922-48-2)
    11. EPA Substance Registry System: 4-(Oxetan-3-yl)butan-1-ol(251922-48-2)

  • 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: 251922-48-2(Hazardous Substances Data)

251922-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 251922-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,1,9,2 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 251922-48:
(8*2)+(7*5)+(6*1)+(5*9)+(4*2)+(3*2)+(2*4)+(1*8)=132
132 % 10 = 2
So 251922-48-2 is a valid CAS Registry Number.

251922-48-2Downstream Products

251922-48-2Relevant articles and documents

Synthesis of extremely simplified compounds possessing the key pharmacophore units of taxol, phenylisoserine and oxetane moieties

Fuji, Kaoru,Watanabe, Yukari,Ohtsubo, Tadamune,Nuruzzaman, Mohammad,Hamajima, Yoshio,Kohno, Michiaki

, p. 1334 - 1337 (2007/10/03)

Straight chain compounds having a phenylisoserine unit and an oxetane ring at the α- and ω- position, respectively as extremely simplified analogues of taxol were prepared. None of these compounds showed promising tubulin inhibitory activity.

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