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4682-50-2

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4682-50-2 Usage

Description

Trichoderonin is a tetracyclic spiroepoxide that functions as an antifungal agent and a protein synthesis inhibitor.

Uses

Used in Pharmaceutical Industry:
Trichoderonin is used as an antifungal agent for its ability to inhibit fungal growth, making it a potential candidate for treating fungal infections.
Used in Agricultural Industry:
Trichoderonin is used as a biocontrol agent for its antifungal properties, helping to protect crops from fungal diseases and promoting healthy plant growth.
Used in Research Applications:
Trichoderonin is used as a protein synthesis inhibitor in research settings to study the mechanisms of protein synthesis and its regulation, contributing to a better understanding of cellular processes and potential therapeutic targets.

Check Digit Verification of cas no

The CAS Registry Mumber 4682-50-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,8 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4682-50:
(6*4)+(5*6)+(4*8)+(3*2)+(2*5)+(1*0)=102
102 % 10 = 2
So 4682-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H24O4/c1-10-5-6-15(3)12(7-10)21-14-8-13(20-11(2)18)16(15,4)17(14)9-19-17/h7,12-14H,5-6,8-9H2,1-4H3/t12-,13-,14-,15+,16-,17-/m1/s1

4682-50-2SDS

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 trichodermin

1.2 Other means of identification

Product number -
Other names 12,13-Epoxytrichothec-9-en-4-ol acetate

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:4682-50-2 SDS

4682-50-2Downstream Products

4682-50-2Relevant articles and documents

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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