Cas 856675-69-9,(S)-4-benzyl-3-((2S,3S,E)-3-hydroxy-2,4-dimethylhex-4-enoyl)oxazolidin-2-one

856675-69-9

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Basic information

Product Name: (S)-4-benzyl-3-((2S,3S,E)-3-hydroxy-2,4-dimethylhex-4-enoyl)oxazolidin-2-one
Synonyms: (S)-4-benzyl-3-((2S,3S,E)-3-hydroxy-2,4-dimethylhex-4-enoyl)oxazolidin-2-one
CAS NO:856675-69-9
Molecular Formula:
Molecular Weight: 317.385
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)-4-benzyl-3-((2S,3S,E)-3-hydroxy-2,4-dimethylhex-4-enoyl)oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-benzyl-3-((2S,3S,E)-3-hydroxy-2,4-dimethylhex-4-enoyl)oxazolidin-2-one(856675-69-9)
EPA Substance Registry System: (S)-4-benzyl-3-((2S,3S,E)-3-hydroxy-2,4-dimethylhex-4-enoyl)oxazolidin-2-one(856675-69-9)

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: 856675-69-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 856675-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,6,7 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 856675-69:
(8*8)+(7*5)+(6*6)+(5*6)+(4*7)+(3*5)+(2*6)+(1*9)=229
229 % 10 = 9
So 856675-69-9 is a valid CAS Registry Number.

856675-69-9Upstream product

856675-69-9Downstream Products

856675-76-8 (S)-4-benzyl-3-((2S,3S,E)-3-(tert-butyl(dimethyl)silyloxy)-2,4-dimethylhex-4-enoyl)oxazolidin-2-one

856675-69-9Relevant academic research and scientific papers

Total synthesis of the potent antitumor polyketide (-)-callystatin A

Dias, Luiz C.,Meira, Paulo R. R.

, p. 4762 - 4773 (2005)

A highly convergent and efficient total synthesis of the potent antitumor polyketide (-)-callystatin A is described. The synthesis required 19 steps from N-propionyl oxazolidinone 23 and produced the desired product in 3.5% overall yield.

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