2777-79-9 Usage
Description
Cevane-3,4,14,15,16,20-hexol, 4,9-epoxy-, 3-acetate, (3beta,4alpha,15alpha,16beta)is an amorphous, steroidal alkaloid that has been isolated from Zygadenus venenosum. Cevane-3,4,14,15,16,20-hexol, 4,9-epoxy-, 3-acetate, (3beta,4alpha,15a lpha,16beta)exhibits a specific rotation of [α]23/sup>D 22° (c 1.53, CHC13). The acetonide form of this compound crystallizes as colorless needles from aqueous Me2CO, with a melting point of 253-5°C (dec.) and a specific rotation of [α]23/sup>D + 2° (c 1.41, CHCl3). It also forms a crystalline hydriodide as colorless plates from Me2CO, with a melting point of 270-1°C (dec.).
Uses
1. Used in Pharmaceutical Industry:
Cevane-3,4,14,15,16,20-hexol, 4,9-epoxy-, 3-acetate, (3beta,4alpha,15alpha,16beta)is used as a pharmaceutical compound due to its steroidal alkaloid nature and unique structural features. Its potential applications may include the development of new drugs targeting various diseases, given its specific interactions and properties.
2. Used in Chemical Research:
Cevane-3,4,14,15,16,20-hexol, 4,9-epoxy-, 3-acetate, (3beta,4alpha,15a lpha,16beta)can be utilized in chemical research for understanding the structure-activity relationships of steroidal alkaloids and their potential applications in various fields, such as medicine, agriculture, and environmental science.
3. Used in Natural Product Chemistry:
Cevane-3,4,14,15,16,20-hexol, 4,9-epoxy-, 3-acetate, (3beta,4alpha,15alpha,16beta)can be employed in the study of natural products, particularly in the context of their isolation, characterization, and potential biological activities.
4. Used in Drug Delivery Systems:
Similar to gallotannin, this compound may also be used in the development of novel drug delivery systems to enhance its applications and efficacy against specific targets or diseases. The unique structural features of this steroidal alkaloid could be exploited to improve drug delivery, bioavailability, and therapeutic outcomes.
Please note that the specific applications and uses mentioned above are hypothetical and based on the general properties of steroidal alkaloids. Further research and experimentation would be required to validate these potential uses.
References
Kupchan, Lavie, Zenis.,J. Amer. Chem. Soc., 77,689 (1953)
Gilbertson., Phytochem., 12,2079 (1973)
Check Digit Verification of cas no
The CAS Registry Mumber 2777-79-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,7 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2777-79:
(6*2)+(5*7)+(4*7)+(3*7)+(2*7)+(1*9)=119
119 % 10 = 9
So 2777-79-9 is a valid CAS Registry Number.
InChI:InChI=1/C29H45NO8/c1-14-5-8-20-26(4,34)22-16(13-30(20)12-14)17-11-27-19(28(17,35)24(33)23(22)32)7-6-18-25(27,3)10-9-21(37-15(2)31)29(18,36)38-27/h14,16-24,32-36H,5-13H2,1-4H3/t14-,16-,17-,18-,19+,20-,21-,22+,23+,24-,25-,26+,27+,28-,29-/m0/s1
