Cas 109050-86-4,3-<3β-acetoxy-5β,17β-dihydroxy-15β,16β-methylene-6α-(phenylseleno)androst-11-en-17α-yl>propionic acid γ-lactone

109050-86-4

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Basic information

Product Name: 3-<3β-acetoxy-5β,17β-dihydroxy-15β,16β-methylene-6α-(phenylseleno)androst-11-en-17α-yl>propionic acid γ-lactone
Synonyms:
CAS NO:109050-86-4
Molecular Formula:
Molecular Weight: 569.6
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-<3β-acetoxy-5β,17β-dihydroxy-15β,16β-methylene-6α-(phenylseleno)androst-11-en-17α-yl>propionic acid γ-lactone(CAS DataBase Reference)
NIST Chemistry Reference: 3-<3β-acetoxy-5β,17β-dihydroxy-15β,16β-methylene-6α-(phenylseleno)androst-11-en-17α-yl>propionic acid γ-lactone(109050-86-4)
EPA Substance Registry System: 3-<3β-acetoxy-5β,17β-dihydroxy-15β,16β-methylene-6α-(phenylseleno)androst-11-en-17α-yl>propionic acid γ-lactone(109050-86-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 109050-86-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109050-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,0,5 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 109050-86:
(8*1)+(7*0)+(6*9)+(5*0)+(4*5)+(3*0)+(2*8)+(1*6)=104
104 % 10 = 4
So 109050-86-4 is a valid CAS Registry Number.

109050-86-4Upstream product

109050-86-4Downstream Products

109050-86-4Relevant academic research and scientific papers

Aldosterone Antagonists. 2. Synthesis and Biological Activities of 11,12-Dehydropregnane Derivatives

Kamata, Susumu,Matsui, Takeaki,Haga, Nobuhiro,Nakamura, Masuhisa,Odaguchi, Kunihiro,et al.

, p. 1647 - 1658 (1987)

Several steroid derivatives having the Δ11-pregnane skeleton with a 17-γ-spirolactone function were synthesized to evaluate their antialdosterone activity and to elucidate the relation between their binding affinity to mineralocorticoid recepto

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