Cas 253677-85-9,(S)-3-{(2R,13R)-13-[(2R,5R)-5-((2S,5R,6S)-6-Decyl-5-hydroxy-tetrahydro-pyran-2-yl)-tetrahydro-furan-2-yl]-2,13-dihydroxy-tridecyl}-5-methyl-5H-furan-2-one

253677-85-9

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Basic information

Product Name: (S)-3-{(2R,13R)-13-[(2R,5R)-5-((2S,5R,6S)-6-Decyl-5-hydroxy-tetrahydro-pyran-2-yl)-tetrahydro-furan-2-yl]-2,13-dihydroxy-tridecyl}-5-methyl-5H-furan-2-one
Synonyms:
CAS NO:253677-85-9
Molecular Formula:
Molecular Weight: 622.927
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)-3-{(2R,13R)-13-[(2R,5R)-5-((2S,5R,6S)-6-Decyl-5-hydroxy-tetrahydro-pyran-2-yl)-tetrahydro-furan-2-yl]-2,13-dihydroxy-tridecyl}-5-methyl-5H-furan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-{(2R,13R)-13-[(2R,5R)-5-((2S,5R,6S)-6-Decyl-5-hydroxy-tetrahydro-pyran-2-yl)-tetrahydro-furan-2-yl]-2,13-dihydroxy-tridecyl}-5-methyl-5H-furan-2-one(253677-85-9)
EPA Substance Registry System: (S)-3-{(2R,13R)-13-[(2R,5R)-5-((2S,5R,6S)-6-Decyl-5-hydroxy-tetrahydro-pyran-2-yl)-tetrahydro-furan-2-yl]-2,13-dihydroxy-tridecyl}-5-methyl-5H-furan-2-one(253677-85-9)

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: 253677-85-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 253677-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,6,7 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 253677-85:
(8*2)+(7*5)+(6*3)+(5*6)+(4*7)+(3*7)+(2*8)+(1*5)=169
169 % 10 = 9
So 253677-85-9 is a valid CAS Registry Number.

253677-85-9Upstream product

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253677-85-9Relevant academic research and scientific papers

Total synthesis of a new cytotoxic acetogenin, jimenezin, and the revised structure.

Takahashi,Maeda,Hirota,Nakata

, p. 2025 - 2028 (1999)

The first total synthesis of jimenezin was achieved by using carbohydrates as chiral building blocks, thus revising the proposed structure 1 to 2. The key steps in this synthesis include an efficient construction of the THP-THF fragments 3 and 16 through

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