Welcome to LookChem.com Sign In|Join Free
  • or
Eubotriol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24338-62-3

Post Buying Request

24338-62-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

24338-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24338-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,3 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24338-62:
(7*2)+(6*4)+(5*3)+(4*3)+(3*8)+(2*6)+(1*2)=103
103 % 10 = 3
So 24338-62-3 is a valid CAS Registry Number.

24338-62-3Relevant academic research and scientific papers

DITERPENES FROM SIDERITIS INFERNALIS

Fernandez, Concepcion,Fraga, Braulio M.,Hernandez, Melchor G.

, p. 2573 - 2576 (1986)

Key Word Index - Sideritis infernalis; Labiatae; diterpenes; ent-kaurene; episinfernal; sinfernal; sinfernol; epoxysinfernol; canditriol.Five new ent-kaurene diterpenes, episinfernal, sinfernal, sinfernol, epoxysinfernol and canditriol, and the known one, candol B, candicandiol and candidiol, have been isolated from the aerial parts of Sideritis infernalis.

THE BIOTRANSFORMATION OF TWO ENT-15β,16β-EPOXY-KAURANE DERIVATIVES BY GIBBERELLA FUJIKUROI

Fraga, Braulio M.,Hernandez, Melchor G.,Garcia-Tellado, Fernando,Gonzalez, Pedro,Peralest, Aurea

, p. 133 - 138 (2007/10/02)

The microbiological transformation of the diterpene ent-15β,16β-epoxy-14α-hydroxykaurane into ent-14α,15β-dihydroxy-11α,16α-epoxykaurane, ent-7α,14α,15β-trihydroxy-11α,16α-epoxykaurane and ent-7β,14α,15β-trihydroxy-11α,16α-epoxykaurane has been carried out using the fungus Gibberella fujikuroi.The incubation with this fungus of sideroxol (ent-7α,18-dihydroxy-15β,16β-epoxykaurane) gave as main products ent-7α,15β,18-trihydroxy-11α,16α-epoxykaurane and ent-7α,13,18-trihydroxy-15α,16α-epoxykaurane.Some of these compounds were identified as their acetate derivatives.The presence of the 15α,16α-epoxy group in these two substrates inhibits transformations involving oxidation at C-9 and favours the hydroxylation at C-11(β).

THE MICROBIOLOGICAL TRANSFORMATION OF SOME ENT-7α,15β-DIHYDROXYKAURENE DERIVATIVES BY GIBBERELLA FUJIKUROI

Fraga, Braulio M.,Hernandez, Melchor G.,Gonzales, Pedro

, p. 2567 - 2571 (2007/10/02)

The microbiological transformation by the fungus Gibberella fujikuroi of ent-7α,15β-dihydroxy-kaur-16-ene gave ent-7α,15β,19-trihydroxy-kaur-16-ene, ent-7α,11α,15β-trihydroxykaur-16-ene, ent-7α,11α,15β,16β,17-pentahydroxy-kaurane and ent-7α,11α,13,15β-tetrahydroxy-kaur-16-ene. ent-7α,15β,18-Trihydroxy-kaur-16-ene (eubotriol) afforded ent-7α,11α,15β,18-tetrahydroxy-kaur-16-ene, ent-7α,15β,18,19-tetrahydroxy-kaur-16-ene, ent-7α,17,18-trihydroxy-15β,16β-epoxy-kaurane (epoxysideritriol), and ent-7α,17,18,19-tetrahydroxy-kaur-15-ene.The last three compounds were identified as their acetate derivatives.Key Word Index - Gibberella fujikuroi; microbiological transformations; diterpenes; ent-7α,15β-dihydroxy-kaur-16-ene; eubotriol.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 24338-62-3