Cas 1172045-80-5,(1R,2R,3S)-3-[(4-methoxybenzyl)oxy]-1-phenyl-2-[(triethylsilyl)oxy]hex-5-en-1-ol

1172045-80-5

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Basic information

Product Name: (1R,2R,3S)-3-[(4-methoxybenzyl)oxy]-1-phenyl-2-[(triethylsilyl)oxy]hex-5-en-1-ol
Synonyms: (1R,2R,3S)-3-[(4-methoxybenzyl)oxy]-1-phenyl-2-[(triethylsilyl)oxy]hex-5-en-1-ol
CAS NO:1172045-80-5
Molecular Formula:
Molecular Weight: 442.671
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: (1R,2R,3S)-3-[(4-methoxybenzyl)oxy]-1-phenyl-2-[(triethylsilyl)oxy]hex-5-en-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,3S)-3-[(4-methoxybenzyl)oxy]-1-phenyl-2-[(triethylsilyl)oxy]hex-5-en-1-ol(1172045-80-5)
EPA Substance Registry System: (1R,2R,3S)-3-[(4-methoxybenzyl)oxy]-1-phenyl-2-[(triethylsilyl)oxy]hex-5-en-1-ol(1172045-80-5)

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: 1172045-80-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1172045-80-5 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, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1172045-80:
(9*1)+(8*1)+(7*7)+(6*2)+(5*0)+(4*4)+(3*5)+(2*8)+(1*0)=125
125 % 10 = 5
So 1172045-80-5 is a valid CAS Registry Number.

1172045-80-5Upstream product

108-86-1 bromobenzene

1172045-80-5Downstream Products

1172046-00-2 (1R,2S,3S)-3-[(4-methoxybenzyl)oxy]-1-phenyl-1,2-bis[(triethylsilyl)oxy]hex-5-ene

1172045-80-5Relevant 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.

, p. 1386 - 1392 (2009)

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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