Cas 84928-46-1,[(3aS4E)-1t-((R)-1,5-dimethyl-hexyl)-7a-methyl-(3ar,7at)-octahydro-inden-4-yliden]-acetaldehyde

84928-46-1

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Basic information

Product Name: [(3aS4E)-1t-((R)-1,5-dimethyl-hexyl)-7a-methyl-(3ar,7at)-octahydro-inden-4-yliden]-acetaldehyde
Synonyms: [(3aS4E)-1t-((R)-1,5-dimethyl-hexyl)-7a-methyl-(3ar,7at)-octahydro-inden-4-yliden]-acetaldehyde
CAS NO:84928-46-1
Molecular Formula:
Molecular Weight: 290.489
EINECS: N/A
Product Categories: N/A
Mol File: 84928-46-1.mol
Article Data: 1

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: [(3aS4E)-1t-((R)-1,5-dimethyl-hexyl)-7a-methyl-(3ar,7at)-octahydro-inden-4-yliden]-acetaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: [(3aS4E)-1t-((R)-1,5-dimethyl-hexyl)-7a-methyl-(3ar,7at)-octahydro-inden-4-yliden]-acetaldehyde(84928-46-1)
EPA Substance Registry System: [(3aS4E)-1t-((R)-1,5-dimethyl-hexyl)-7a-methyl-(3ar,7at)-octahydro-inden-4-yliden]-acetaldehyde(84928-46-1)

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: 84928-46-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 84928-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,2 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84928-46:
(7*8)+(6*4)+(5*9)+(4*2)+(3*8)+(2*4)+(1*6)=171
171 % 10 = 1
So 84928-46-1 is a valid CAS Registry Number.

84928-46-1Upstream product

67-97-0 vitamin D₃

84928-46-1Downstream Products

67-97-0 vitamin D₃

84928-46-1Relevant articles and documents

Synthesis of a novel class of cdc25A inhibitors from Vitamin D3

Dodo, Kosuke,Takahashi, Masato,Yamada, Yuji,Sugimoto, Yoshikazu,Hashimoto, Yuichi,Shirai, Ryuichi

, p. 615 - 617 (2000)

We have developed a novel class of cdc25A inhibitors by drastic modification of hydrophobic and hydrophillic substructures of dysidiolide. The unsaturated derivative 3b strongly inhibited cdc25A (IC50=7.7 μM) and caused G1 arrest of HL60 cells. (C) 2000 Elsevier Science Ltd. All rights reserved.

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