Beta-Tetralone

CAS No. 530-93-8

Beta-Tetralone( beta-Tetralone | AI3-12003 | AI3 12003 | AI312003 )

Catalog No. M14885 CAS No. 530-93-8

2-Tetralone is an organic chemical compound with the molecular formula C10H10O.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 28 In Stock
50MG 36 In Stock
100MG 48 In Stock
200MG Get Quote In Stock
500MG 110 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Beta-Tetralone
  • Note
    Research use only, not for human use.
  • Brief Description
    2-Tetralone is an organic chemical compound with the molecular formula C10H10O.
  • Description
    2-Tetralone is an organic chemical compound with the molecular formula C10H10O. This colourless oil is an intermediate in organic synthesis. It is a ketone derivative of tetralin, a hydrogenated derivative of naphthalene. A related compound is 1-tetralone.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    beta-Tetralone | AI3-12003 | AI3 12003 | AI312003
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    P450
  • Recptor
    CYP2A
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    530-93-8
  • Formula Weight
    146.19
  • Molecular Formula
    C10H10O
  • Purity
    >98% (HPLC)
  • Solubility
    Soluble in DMSO
  • SMILES
    O=C1CC2=C(C=CC=C2)CC1
  • Chemical Name
    1,2,3,4-Tetrahydronaphthalen-2-one

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.ADKINS H, et al. J Am Chem Soc. 1948 Dec;70(12):4247.
molnova catalog
related products
  • 7-BFC

    7-BFC (7-Benzyloxy-4-(trifluoromethyl)coumarin) is a coumarin-like fluorescent substrate that serves as a biomarker for cytochrome P 450 and can be used to study CYP isoforms and cytochrome P 450 metabolism.

  • CAY10434

    CAY10434 is an active inhibitor of CYP4A hydroxylase with an IC50 value of 8.8 nM in human kidney microsomal test.

  • Praeruptorin A (b)

    Praeruptorin A could exhibit its anti-osteoclastogenic activity by inhibiting p38/Akt-c-Fos-NFATc1 signaling and PLCγ-independent Ca(2+) oscillation.