Cas 77877-26-0,(4R,5S)-3-((2R,3R)-3-Hydroxy-2-methyl-3-phenyl-propionyl)-4-methyl-5-phenyl-oxazolidin-2-one

77877-26-0

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Basic information

Product Name: (4R,5S)-3-((2R,3R)-3-Hydroxy-2-methyl-3-phenyl-propionyl)-4-methyl-5-phenyl-oxazolidin-2-one
Synonyms: (4R,5S)-3-((2R,3R)-3-Hydroxy-2-methyl-3-phenyl-propionyl)-4-methyl-5-phenyl-oxazolidin-2-one
CAS NO:77877-26-0
Molecular Formula:
Molecular Weight: 339.391
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: (4R,5S)-3-((2R,3R)-3-Hydroxy-2-methyl-3-phenyl-propionyl)-4-methyl-5-phenyl-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5S)-3-((2R,3R)-3-Hydroxy-2-methyl-3-phenyl-propionyl)-4-methyl-5-phenyl-oxazolidin-2-one(77877-26-0)
EPA Substance Registry System: (4R,5S)-3-((2R,3R)-3-Hydroxy-2-methyl-3-phenyl-propionyl)-4-methyl-5-phenyl-oxazolidin-2-one(77877-26-0)

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: 77877-26-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 77877-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,7 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77877-26:
(7*7)+(6*7)+(5*8)+(4*7)+(3*7)+(2*2)+(1*6)=190
190 % 10 = 0
So 77877-26-0 is a valid CAS Registry Number.

77877-26-0Upstream product

77877-26-0Downstream Products

76549-05-8 methyl (2R,3R)-3-hydroxy-2-methyl-3-phenylpropanoate

77877-26-0Relevant academic research and scientific papers

On the reversal of the stereoselectivity in the Evans aldol reaction of α-amino aldehydes

Hayashi,Hamada,Shioiri

, p. 7287 - 7290 (2007/10/02)

Reversal of the stereoselectivity in the Evans aldol reaction of Boc-(S)-prolinal (3), observed during the total synthesis of dolastatin 10 (1), was proved to be due to the amounts of dibutylboron triflate and triethylamine. (R)-Alaninal derivatives (14)

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