Cas 1278519-75-7,(R)-8-(4-methoxybenzyloxy)-7-methyl-3-((S)-1-(2-((R)-pent-4-yn-2-yl)oxazol-4-yl)propan-2-yl)isochroman-1-one

1278519-75-7

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Basic information

Product Name: (R)-8-(4-methoxybenzyloxy)-7-methyl-3-((S)-1-(2-((R)-pent-4-yn-2-yl)oxazol-4-yl)propan-2-yl)isochroman-1-one
Synonyms: (R)-8-(4-methoxybenzyloxy)-7-methyl-3-((S)-1-(2-((R)-pent-4-yn-2-yl)oxazol-4-yl)propan-2-yl)isochroman-1-one
CAS NO:1278519-75-7
Molecular Formula:
Molecular Weight: 473.569
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: (R)-8-(4-methoxybenzyloxy)-7-methyl-3-((S)-1-(2-((R)-pent-4-yn-2-yl)oxazol-4-yl)propan-2-yl)isochroman-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (R)-8-(4-methoxybenzyloxy)-7-methyl-3-((S)-1-(2-((R)-pent-4-yn-2-yl)oxazol-4-yl)propan-2-yl)isochroman-1-one(1278519-75-7)
EPA Substance Registry System: (R)-8-(4-methoxybenzyloxy)-7-methyl-3-((S)-1-(2-((R)-pent-4-yn-2-yl)oxazol-4-yl)propan-2-yl)isochroman-1-one(1278519-75-7)

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: 1278519-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1278519-75-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,8,5,1 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1278519-75:
(9*1)+(8*2)+(7*7)+(6*8)+(5*5)+(4*1)+(3*9)+(2*7)+(1*5)=197
197 % 10 = 7
So 1278519-75-7 is a valid CAS Registry Number.

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1278519-75-7Relevant academic research and scientific papers

Total synthesis of 8-deshydroxyajudazol B

Birkett, Stephen,Ganame, Danny,Hawkins, Bill C.,Meiries, Sebastien,Quach, Tim,Rizzacasa, Mark A.

, p. 1964 - 1967 (2011)

The total synthesis of a stereoisomer of 8-deshydroxyajudazol B (4), the putative biosynthetic intermediate of the ajudazols A (1) and B (2), is described. The key steps in the synthesis included an intramolecular Diels-Alder (IMDA) reaction to secure the

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