Cas 1454816-39-7,(S)-2-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyloctahydro-1H-inden-1-yl)propyl cyclohexanecarboxylate

1454816-39-7

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Basic information

Product Name: (S)-2-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyloctahydro-1H-inden-1-yl)propyl cyclohexanecarboxylate
Synonyms: (S)-2-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyloctahydro-1H-inden-1-yl)propyl cyclohexanecarboxylate
CAS NO:1454816-39-7
Molecular Formula:
Molecular Weight: 322.488
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: (S)-2-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyloctahydro-1H-inden-1-yl)propyl cyclohexanecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyloctahydro-1H-inden-1-yl)propyl cyclohexanecarboxylate(1454816-39-7)
EPA Substance Registry System: (S)-2-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyloctahydro-1H-inden-1-yl)propyl cyclohexanecarboxylate(1454816-39-7)

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: 1454816-39-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1454816-39-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,4,8,1 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1454816-39:
(9*1)+(8*4)+(7*5)+(6*4)+(5*8)+(4*1)+(3*6)+(2*3)+(1*9)=177
177 % 10 = 7
So 1454816-39-7 is a valid CAS Registry Number.

1454816-39-7Upstream product

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1454816-39-7Relevant academic research and scientific papers

Analogues of the Inhoffen-Lythgoe diol with anti-proliferative activity

Deberardinis, Albert M.,Lemieux, Steven,Hadden, M. Kyle

, p. 5367 - 5370 (2013)

The anti-proliferative activity of a series of ester- and amide-linked Inhoffen-Lythgoe side chain analogues is reported. Whereas the Inhoffen-Lythgoe diol was inactive in these studies, a number of aromatic and aliphatic ester-linked side chains demonstr

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