562-71-0 Usage
Description
(8R,19R,22E)-7α,19:8,19-Dicyclo-9,10-secoergosta-5(10),22-dien-2α-ol is a complex organic compound that belongs to the secoergostane class of sterols. It is characterized by a steroid nucleus with a cycloheptane ring system and features a double bond at position 22 and hydroxyl groups at positions 7 and 2. This specific chemical is a type of ergosterol, which is an essential component in the growth and development of fungi and serves as a precursor for the synthesis of vital molecules such as vitamin D2 and various steroidal hormones.
Uses
Used in Pharmaceutical Research:
(8R,19R,22E)-7α,19:8,19-Dicyclo-9,10-secoergosta-5(10),22-dien-2α-ol is used as a target compound in pharmaceutical research for its role in the growth and development of fungi. Its involvement in the synthesis of essential molecules like vitamin D2 and steroidal hormones makes it a significant focus for the development of new drugs and therapies.
Used in Antifungal Applications:
In the field of antifungal research, (8R,19R,22E)-7α,19:8,19-Dicyclo-9,10-secoergosta-5(10),22-dien-2α-ol is used as a key component in the development of antifungal drugs and compounds. Its presence in the synthesis of ergosterol, which has been implicated in the antifungal properties of certain medications, makes it an important target for creating new and effective treatments against fungal infections.
Used in Vitamin D2 Synthesis:
(8R,19R,22E)-7α,19:8,19-Dicyclo-9,10-secoergosta-5(10),22-dien-2α-ol is used as a precursor in the synthesis of vitamin D2, which is an essential nutrient for maintaining healthy bones and immune system function. Its role in the production of this vital compound makes it a valuable resource in the field of nutrition and supplementation.
Used in Steroidal Hormone Production:
This specific chemical is also used as a precursor in the production of various steroidal hormones, which play a crucial role in regulating numerous physiological processes in the body. Its involvement in hormone synthesis highlights its importance in the development of pharmaceuticals for hormone-related conditions and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 562-71-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 562-71:
(5*5)+(4*6)+(3*2)+(2*7)+(1*1)=70
70 % 10 = 0
So 562-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C28H44O/c1-17(2)18(3)7-8-19(4)23-11-12-25-27(23,5)13-6-14-28(25)24-15-20-9-10-21(29)16-22(20)26(24)28/h7-8,17-19,21,23-26,29H,6,9-16H2,1-5H3/b8-7+/t18-,19+,21-,23+,24-,25+,26+,27+,28?/m0/s1