Stable Isotopes Product Detail

Algestone Acetonide-d6

Chemical Properties and Information

Product Code: CS-T-96728 Stable Isotopes
Algestone Acetonide-d6
API Family
Algestone
Product Code
CS-T-96728

Algestone Acetonide-d6

Algestone Stable Isotopes
Stock Status: : Enquire Live

CAT No.
CS-T-96728
CAS No.
--
Molecular Formula
C₂₄H₂₈D₆O₄
Molecular Weight
392.56
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There is no hazardous surcharge associated with this product.
There is no packaging charge associated with this product.
For Research Purposes only. Not for Personal use.
All compounds supplied are strictly intended for laboratory, research, analytical, and scientific use only. They are not meant for human consumption, therapeutic use, or any form of clinical application.
CAS No.
-
Product Code
CS-T-96728
M.F.
C24H28D6O4
M.W.
392.56
Smiles
O=C1CC[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@]5(C(C)=O)OC(C([2H])([2H])[2H])(C([2H])([2H])[2H])O[C@]5([H])C[C@@]4([H])[C@]3([H])CCC2=C1
Category
Stable Isotopes
API Family
Algestone
Storage Condition
Refer MSDS for complete information.
IUPAC Name
(1R,2S,4R,8S,9S,12S,13R)-8-acetyl-9,13-dimethyl-6,6-bis(trideuteriomethyl)-5,7-dioxapentacyclo[10.8.0.02,9.04,8.013,18]icos-17-en-16-one
References
"Golikov, P., et al.: Endokrinologie, 80, 18 (1982); Korkhov, V., et al.: Voprosy Okhrany Materinstva i Detstva, 25, 74 (1980)"
Synonyms
(1R,2S,4R,8S,9S,12S,13R)-8-acetyl-9,13-dimethyl-6,6-bis(trideuteriomethyl)-5,7-dioxapentacyclo[10.8.0.02,9.04,8.013,18]icos-17-en-16-one
Application Notes
"Algestone Acetonide-d6 is the labelled form of Algestone acetonide, which is a steroid that can surppress [3H]uridine from being included into thymocyte RNA. Algestone acetonide had estrogenic activity and acted as a contraceptive when combined with mestranol in ovariectomized rabbits and rats."
Hazard Compound
Refer MSDS for complete information.
Overview
"Algestone Acetonide-d6 is the labelled form of Algestone acetonide, which is a steroid that can surppress [3H]uridine from being included into thymocyte RNA. Algestone acetonide had estrogenic activity and acted as a contraceptive when combined with mestranol in ovariectomized rabbits and rats."
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