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4-hydroxy-3-(tetrahydro-2H-pyran-2-yloxy)-12,13-epoxytrichothec-9-en-15-yl acetate is a complex organic compound with the molecular formula C19H26O6. It is a derivative of the trichotecane sesquiterpene class, characterized by the presence of a hydroxyl group at the 4-position, a tetrahydro-2H-pyran-2-yloxy group at the 3-position, and an epoxy group between the 12 and 13 positions. The compound also features a 9-en double bond and a 15-yl acetate group, which is an acetate ester attached to the 15-carbon position. This chemical structure is significant in the field of organic chemistry, particularly in the study of natural products and their synthetic analogs, as it may exhibit unique biological activities or be used as an intermediate in the synthesis of other compounds.

77620-42-9

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77620-42-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77620-42-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,2 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77620-42:
(7*7)+(6*7)+(5*6)+(4*2)+(3*0)+(2*4)+(1*2)=139
139 % 10 = 9
So 77620-42-9 is a valid CAS Registry Number.

77620-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 12,13-epoxy-4β-hydroxy-3α-<(tetrahydro-2H-pyranyl)oxy>trichothec-9-en-15-yl acetate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:77620-42-9 SDS

77620-42-9Relevant academic research and scientific papers

Synthesis and biological activity of C-4 and C-15 Aryl azide derivatives of anguidine

Richardson, Stewart K.,Jeganathan, Alwarsamy,Mani, Rajarathnam S.,Haley, Boyd E.,Watt, David S.,Trusal, Lynn R.

, p. 2925 - 2934 (2007/10/02)

Potential trichothecene photoaffinity reagents were prepared by coupling either the C-4 or C-15 alcohols derived from anguidine with (3-azido-5-methoxyphenoxy) acetic acid, 4-(3-azido-5-methoxyphenoxy)butyric acid, or N-(3-azido-5-methoxyphenyl) N'-(carbo

CONVERSION OF ANGUIDINE INTO CALONECTRIN AND 3-DEACETYL-CALONECTRIN

Jeker, Nicolas,Mohr, Peter,Tamm, Christoph

, p. 5637 - 5640 (2007/10/02)

Anguidine (diacetoxyscirpenol, 2) was converted into calonectrin (3) in 7 steps using the Barton deoxygenation as key reaction.

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