Cas 1189128-47-9,(2S,4S,5S,6E)-2-tert-butyldimethylsilyloxy-4-phenylthio-5-triethylsilyloxy-6-octen-3-one

1189128-47-9

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Basic information

Product Name: (2S,4S,5S,6E)-2-tert-butyldimethylsilyloxy-4-phenylthio-5-triethylsilyloxy-6-octen-3-one
Synonyms: (2S,4S,5S,6E)-2-tert-butyldimethylsilyloxy-4-phenylthio-5-triethylsilyloxy-6-octen-3-one
CAS NO:1189128-47-9
Molecular Formula:
Molecular Weight: 494.886
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: (2S,4S,5S,6E)-2-tert-butyldimethylsilyloxy-4-phenylthio-5-triethylsilyloxy-6-octen-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4S,5S,6E)-2-tert-butyldimethylsilyloxy-4-phenylthio-5-triethylsilyloxy-6-octen-3-one(1189128-47-9)
EPA Substance Registry System: (2S,4S,5S,6E)-2-tert-butyldimethylsilyloxy-4-phenylthio-5-triethylsilyloxy-6-octen-3-one(1189128-47-9)

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: 1189128-47-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1189128-47-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,9,1,2 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1189128-47:
(9*1)+(8*1)+(7*8)+(6*9)+(5*1)+(4*2)+(3*8)+(2*4)+(1*7)=179
179 % 10 = 9
So 1189128-47-9 is a valid CAS Registry Number.

1189128-47-9Upstream product

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1189128-47-9Relevant academic research and scientific papers

Stereoselective synthesis of highly functionalized structures from lactate-derived halo ketones

Nebot, Joaquim,Romea, Pedro,Urpi, Felix

, p. 7518 - 7521 (2009)

(Chemical Equation Presented) Highly diastereoselective (i-PrO) 2TiCl2-mediated aldol reactions from lactate-derived α′-halo α-silyloxy ketones and subsequent treatment of the resultant aldols with a wide range of nucleophiles furnis

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