Cas 118745-24-7,(S)-3-hydroxy-1-phenyl-3-((4R,4'R,5R)-2,2,2',2'-tetramethyl-4,4'-bi(1,3-dioxolan)-5-yl)propan-1-one

118745-24-7

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Basic information

Product Name: (S)-3-hydroxy-1-phenyl-3-((4R,4'R,5R)-2,2,2',2'-tetramethyl-4,4'-bi(1,3-dioxolan)-5-yl)propan-1-one
Synonyms: (S)-3-hydroxy-1-phenyl-3-((4R,4'R,5R)-2,2,2',2'-tetramethyl-4,4'-bi(1,3-dioxolan)-5-yl)propan-1-one
CAS NO:118745-24-7
Molecular Formula:
Molecular Weight: 350.412
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: (S)-3-hydroxy-1-phenyl-3-((4R,4'R,5R)-2,2,2',2'-tetramethyl-4,4'-bi(1,3-dioxolan)-5-yl)propan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-hydroxy-1-phenyl-3-((4R,4'R,5R)-2,2,2',2'-tetramethyl-4,4'-bi(1,3-dioxolan)-5-yl)propan-1-one(118745-24-7)
EPA Substance Registry System: (S)-3-hydroxy-1-phenyl-3-((4R,4'R,5R)-2,2,2',2'-tetramethyl-4,4'-bi(1,3-dioxolan)-5-yl)propan-1-one(118745-24-7)

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: 118745-24-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 118745-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,7,4 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 118745-24:
(8*1)+(7*1)+(6*8)+(5*7)+(4*4)+(3*5)+(2*2)+(1*4)=137
137 % 10 = 7
So 118745-24-7 is a valid CAS Registry Number.

118745-24-7Upstream product

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118745-24-7Relevant academic research and scientific papers

Stereoselective direct amine-catalyzed decarboxylative aldol addition

Rohr, Kerstin,Mahrwald, Rainer

supporting information; experimental part, p. 1878 - 1880 (2011/06/20)

A stereoselective decarboxylative aldol addition of β- and α-keto acids in the presence of catalytic amounts of amines is described. By the optional deployment of chiral enolizable aldehydes an access to enantiopure configurative defined ketopentoses, ketohexoses, or ketoheptoses is given.

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