Cas 1172045-79-2,(1S,2R,6S)-6-{2-phenyl-1,2-bis[(triethylsilyl)oxy]ethyl}-5,6-dihydro-2H-pyran-2-one

1172045-79-2

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Basic information

Product Name: (1S,2R,6S)-6-{2-phenyl-1,2-bis[(triethylsilyl)oxy]ethyl}-5,6-dihydro-2H-pyran-2-one
Synonyms: (1S,2R,6S)-6-{2-phenyl-1,2-bis[(triethylsilyl)oxy]ethyl}-5,6-dihydro-2H-pyran-2-one
CAS NO:1172045-79-2
Molecular Formula:
Molecular Weight: 462.777
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: (1S,2R,6S)-6-{2-phenyl-1,2-bis[(triethylsilyl)oxy]ethyl}-5,6-dihydro-2H-pyran-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,6S)-6-{2-phenyl-1,2-bis[(triethylsilyl)oxy]ethyl}-5,6-dihydro-2H-pyran-2-one(1172045-79-2)
EPA Substance Registry System: (1S,2R,6S)-6-{2-phenyl-1,2-bis[(triethylsilyl)oxy]ethyl}-5,6-dihydro-2H-pyran-2-one(1172045-79-2)

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: 1172045-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1172045-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,2,0,4 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1172045-79:
(9*1)+(8*1)+(7*7)+(6*2)+(5*0)+(4*4)+(3*5)+(2*7)+(1*9)=132
132 % 10 = 2
So 1172045-79-2 is a valid CAS Registry Number.

1172045-79-2Upstream product

1172046-05-7 (1R,2S,3S)-1-phenyl-1,2-bis[(triethylsilyl)oxy]hex-5-en-3-yl prop-2-enoate

1172045-79-2Downstream Products

1172045-79-2Relevant academic research and scientific papers

Stereoselective total syntheses of leiocarpin A and (-)-galantinic acid starting from D-mannitol

Nagaiah, Kommu,Sreenu, Domalapally,Purnima, Kamaraju V.,Rao, Ramisetti Srinivasa,Yadav, Jhillu S.

experimental part, p. 1386 - 1392 (2010/01/15)

Stereoselective total syntheses of leiocarpin A and (-)-galantinic acid, starting from D-mannitol as a chiral synthon, are described. The key steps involve stereoselective allylations, a Grignard reaction to control the required stereogenic centers, and r

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