Cas 205253-49-2,4(R)-benzyl-3-[(2R,3S,4R,5S)-5-(tert-butyldimethylsilanyloxy)-3-hydroxy-2,4-dimethylheptanoyl]oxazolidin-2-one

205253-49-2

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Basic information

Product Name: 4(R)-benzyl-3-[(2R,3S,4R,5S)-5-(tert-butyldimethylsilanyloxy)-3-hydroxy-2,4-dimethylheptanoyl]oxazolidin-2-one
Synonyms: 4(R)-benzyl-3-[(2R,3S,4R,5S)-5-(tert-butyldimethylsilanyloxy)-3-hydroxy-2,4-dimethylheptanoyl]oxazolidin-2-one
CAS NO:205253-49-2
Molecular Formula:
Molecular Weight: 463.69
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: 4(R)-benzyl-3-[(2R,3S,4R,5S)-5-(tert-butyldimethylsilanyloxy)-3-hydroxy-2,4-dimethylheptanoyl]oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 4(R)-benzyl-3-[(2R,3S,4R,5S)-5-(tert-butyldimethylsilanyloxy)-3-hydroxy-2,4-dimethylheptanoyl]oxazolidin-2-one(205253-49-2)
EPA Substance Registry System: 4(R)-benzyl-3-[(2R,3S,4R,5S)-5-(tert-butyldimethylsilanyloxy)-3-hydroxy-2,4-dimethylheptanoyl]oxazolidin-2-one(205253-49-2)

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: 205253-49-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 205253-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,2,5 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 205253-49:
(8*2)+(7*0)+(6*5)+(5*2)+(4*5)+(3*3)+(2*4)+(1*9)=102
102 % 10 = 2
So 205253-49-2 is a valid CAS Registry Number.

205253-49-2Upstream product

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205253-49-2Relevant academic research and scientific papers

Substrate recognition and channeling of monomodules from the pikromycin polyketide synthase

Beck, Brian J.,Aldrich, Courtney C.,Fecik, Robert A.,Reynolds, Kevin A.,Sherman, David H.

, p. 12551 - 12557 (2003)

The unique ability of the pikromycin (Pik) polyketide synthase to generate 12- and 14-membered ring macrolactones presents an opportunity to explore the fundamental processes underlying polyketide synthesis, specifically the mechanistic details of the cha

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