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80178-17-2

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80178-17-2 Usage

Description

(3beta)-3,15-dihydroxy-12,13-epoxytrichothec-9-en-4-yl chloroacetate is a potent mycotoxin belonging to the trichothecene group, produced by certain molds such as Fusarium and Myrothecium species. It is a hazardous chemical compound that poses significant health risks to humans and animals through exposure to contaminated grains and agricultural products.

Uses

Used in Toxicological Research:
(3beta)-3,15-dihydroxy-12,13-epoxytrichothec-9-en-4-yl chloroacetate is used as a subject of toxicological research to study its cytotoxic and immunosuppressive effects, as well as its role in causing gastrointestinal disturbances, skin irritation, and respiratory issues. Understanding its toxicological effects helps in developing methods to monitor and limit exposure to this harmful compound.
Used in Agricultural Monitoring:
(3beta)-3,15-dihydroxy-12,13-epoxytrichothec-9-en-4-yl chloroacetate is used as a target for monitoring and detection in agricultural products to ensure food safety and prevent contamination. Efforts are made to control and reduce the presence of this toxin in grains and other crops to protect both human and animal health.
Used in Environmental Health:
(3beta)-3,15-dihydroxy-12,13-epoxytrichothec-9-en-4-yl chloroacetate is used as an indicator of environmental health risks associated with mold contamination. Its presence in the environment can signify the need for interventions to improve air quality and reduce exposure to hazardous substances.

Check Digit Verification of cas no

The CAS Registry Mumber 80178-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,7 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80178-17:
(7*8)+(6*0)+(5*1)+(4*7)+(3*8)+(2*1)+(1*7)=122
122 % 10 = 2
So 80178-17-2 is a valid CAS Registry Number.

80178-17-2Downstream Products

80178-17-2Relevant articles and documents

Structural modifications of anguidin and antitumor activities of its analogues

Kaneko,Schmitz,Essery,Rose,Howell,O'Herron,Nachfolger,Huftalen,Bradner,Partyka,Doyle,Davies,Cundliffe

, p. 579 - 589 (2007/10/02)

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