2506-60-7 Usage
General Description
The chemical (1S,3aS,3bR,7aR,8aS,8bS,8cS,10aS)-8b,10a-dimethyl-7-oxo-1,2,3,3a,3b,4,5,7,7a,8,8a,8b,8c,9,10,10a-hexadecahydrocyclopenta[a]cyclopropa[g]phenanthren-1-yl acetate is a complex organic compound with a long and specific molecular structure. It is an acetate derivative of a cyclopentacyclopropa[g]phenanthrene, and the presence of the acetate group indicates that it contains an acetyl functional group. The compound also contains multiple methyl groups and a ketone group, which are likely to contribute to its chemical properties and reactivity. This chemical may have potential uses in various industrial and pharmaceutical applications, but its specific functions and effects would require further research and analysis.
Check Digit Verification of cas no
The CAS Registry Mumber 2506-60-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,0 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2506-60:
(6*2)+(5*5)+(4*0)+(3*6)+(2*6)+(1*0)=67
67 % 10 = 7
So 2506-60-7 is a valid CAS Registry Number.
2506-60-7Relevant articles and documents
The Reaction of Some 1α,2α- and 2α,3α-Methylene Steroids with Hydrobromic Acid
Hanson, James R.,Knights, Steve G.
, p. 24 - 28 (2007/10/02)
Treatment of 17β-acetoxy-methyleneandrost-4-en-3-one under the conditions of the dienone-phenol rearrangement affords 17β-acetoxy-1α-bromomethylandrost-4-en-3-one rather than a phenol.The corresponding 3α-alcohol gave a 1α-bromothexyl-3,5-diene rather than an aromatic compounds. 2α,3α-methyleneandrost-5-ene-4,17-dione also gave a 2α-bromomethylandrost-5-ene-4,17-dione rather than a phenol.
