Cas 454473-87-1,(1R,2R,4aR,8aR)-1,2,4a,5,6,7,8,8a-octahydro-2-methylnaphthalene-1-carboxylic acid

454473-87-1

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Basic information

Product Name: (1R,2R,4aR,8aR)-1,2,4a,5,6,7,8,8a-octahydro-2-methylnaphthalene-1-carboxylic acid
Synonyms: (1R,2R,4aR,8aR)-1,2,4a,5,6,7,8,8a-octahydro-2-methylnaphthalene-1-carboxylic acid
CAS NO:454473-87-1
Molecular Formula:
Molecular Weight: 194.274
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: (1R,2R,4aR,8aR)-1,2,4a,5,6,7,8,8a-octahydro-2-methylnaphthalene-1-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,4aR,8aR)-1,2,4a,5,6,7,8,8a-octahydro-2-methylnaphthalene-1-carboxylic acid(454473-87-1)
EPA Substance Registry System: (1R,2R,4aR,8aR)-1,2,4a,5,6,7,8,8a-octahydro-2-methylnaphthalene-1-carboxylic acid(454473-87-1)

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: 454473-87-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 454473-87-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,4,4,7 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 454473-87:
(8*4)+(7*5)+(6*4)+(5*4)+(4*7)+(3*3)+(2*8)+(1*7)=171
171 % 10 = 1
So 454473-87-1 is a valid CAS Registry Number.

454473-87-1Upstream product

550334-72-0 (4R)-benzyl-3-((1R,2R,4aS,8aR)-1,2,4a,5,6,7,8,8a-octahydro-2-methylnaphthalene-1-carbonyl)oxazolidin-2-one

454473-87-1Downstream Products

454473-87-1Relevant academic research and scientific papers

Toward the synthesis of tetrodecamycin: Asymmetric synthesis of a direct precursor of the C6-C18 trans-decalin portion

Paintner, Franz F.,Bauschke, Gerd,Polborn, Kurt

, p. 2549 - 2552 (2003)

We report the asymmetric synthesis of a direct precursor of the C6-C18 trans-decalin portion of tetrodecamycin utilising an asymmetric intramolecular Diels-Alder (IMDA) reaction as the key step.

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