Cas 79320-89-1,15-acetoxy-3-hydroxy-3,4-O,O-ethylidene-12,13-epoxytrichothec-9-ene

79320-89-1

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Basic information

Product Name: 15-acetoxy-3-hydroxy-3,4-O,O-ethylidene-12,13-epoxytrichothec-9-ene
Synonyms: 15-acetoxy-3-hydroxy-3,4-O,O-ethylidene-12,13-epoxytrichothec-9-ene
CAS NO:79320-89-1
Molecular Formula: C19H26O7
Molecular Weight: 366.4055
EINECS: N/A
Product Categories: N/A
Mol File: 79320-89-1.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: 488.5°Cat760mmHg
Flash Point: 171.6°C
Appearance: /
Density: 1.36g/cm³
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 15-acetoxy-3-hydroxy-3,4-O,O-ethylidene-12,13-epoxytrichothec-9-ene(CAS DataBase Reference)
NIST Chemistry Reference: 15-acetoxy-3-hydroxy-3,4-O,O-ethylidene-12,13-epoxytrichothec-9-ene(79320-89-1)
EPA Substance Registry System: 15-acetoxy-3-hydroxy-3,4-O,O-ethylidene-12,13-epoxytrichothec-9-ene(79320-89-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 79320-89-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79320-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,2 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79320-89:
(7*7)+(6*9)+(5*3)+(4*2)+(3*0)+(2*8)+(1*9)=151
151 % 10 = 1
So 79320-89-1 is a valid CAS Registry Number.

79320-89-1Upstream product

2269-44-5 3-ketoanguidin

79320-89-1Downstream Products

79320-89-1Relevant articles and documents

Reductive amination of 3-Ketoanguidin and Antitumor Activity of the Products

Kaneko, T.,Wong, H.,Howell, H. G.,Rose, W. C.,Bradner, W. T.,Doyle, T. W.

, p. 958 - 960 (2007/10/02)

Amine-containing trichothecanes were prepared by reductive aminations of 3-ketoanguidin.In in vivo tests against P388 leukemia, most of them showed an improved activity compared to anguidin though their potency was decreased. 3-Ketoanguidin also produced some unexpected structures: oxazoline 5, dioxaline 7, and α-amino nitrile 13.

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