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4,15-Diacetylverrucarol is a chemical compound derived from verrucarol, a sesquiterpene lactone found in various fungi species. It is formed by the acetylation of verrucarol at the 4 and 15 positions, resulting in an increased molecular weight and altered chemical properties. This modification can lead to changes in its biological activity, such as antifungal, antibacterial, or cytotoxic effects. The compound is of interest in the field of natural products chemistry and may have potential applications in pharmaceuticals or agrochemicals due to its bioactivity. However, further research is needed to fully understand its properties and potential uses.

2198-94-9

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2198-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2198-94-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,9 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2198-94:
(6*2)+(5*1)+(4*9)+(3*8)+(2*9)+(1*4)=99
99 % 10 = 9
So 2198-94-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H26O6/c1-11-5-6-18(9-22-12(2)20)15(7-11)25-16-8-14(24-13(3)21)17(18,4)19(16)10-23-19/h7,14-16H,5-6,8-10H2,1-4H3/t14?,15-,16?,17-,18-,19?/m1/s1

2198-94-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Trichothec-9-ene-4,15-diol,12,13-epoxy-,diacetate

1.2 Other means of identification

Product number -
Other names 4,15-Diacetylverrucarol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2198-94-9 SDS

2198-94-9Relevant academic research and scientific papers

Synthesis of Trichoverrin B and Its Conversion to Verrucarin J

Esmond, Robert,Fraser-Reid, Bert,Jarvis, Bruce B.

, p. 3358 - 3360 (2007/10/02)

Anguidine (3b) was converted to verrucarol (3a), which in turn was selectively acylated to yield trichoverin B (2).Trichoverrin B reacts with pyridinium dichromate in dimethylformamide, via a novel oxidative ring closure, to give verrucarin J (11a) in 50 percent yield.

The ready conversion of anguidine into verrucarol and trichodermol

Tulshian, Deen Bandhu,Fraser-Reid, Bert

, p. 4549 - 4552 (2007/10/02)

Anguidine, 1, is readily converted into verrucarol diacetate, 2d, in 85 percent yield by application of the Barton-McCombie deoxygenation procedure. To enable conversion into trichodermol, 3a, the primary hydroxyl group of verrucarol, 2a, is selectively acetylated or is selectively acetylated or preferably silylated, thereby paving the way for its deoxygenation in three simple, high-yield reactions.

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