Cas 389634-52-0,(2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol (S)-2-(1-hydroxy-2-trimethylsilylethyl)-3-furanylboronate

389634-52-0

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Basic information

Product Name: (2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol (S)-2-(1-hydroxy-2-trimethylsilylethyl)-3-furanylboronate
Synonyms: (2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol (S)-2-(1-hydroxy-2-trimethylsilylethyl)-3-furanylboronate
CAS NO:389634-52-0
Molecular Formula:
Molecular Weight: 646.663
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: (2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol (S)-2-(1-hydroxy-2-trimethylsilylethyl)-3-furanylboronate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol (S)-2-(1-hydroxy-2-trimethylsilylethyl)-3-furanylboronate(389634-52-0)
EPA Substance Registry System: (2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol (S)-2-(1-hydroxy-2-trimethylsilylethyl)-3-furanylboronate(389634-52-0)

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: 389634-52-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 389634-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,6,3 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 389634-52:
(8*3)+(7*8)+(6*9)+(5*6)+(4*3)+(3*4)+(2*5)+(1*2)=200
200 % 10 = 0
So 389634-52-0 is a valid CAS Registry Number.

389634-52-0Upstream product

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389634-52-0Relevant academic research and scientific papers

Diastereoselective addition reactions of furyl aldehydes using chiral boronates as auxiliary: Application to the enantioselective synthesis of 2,3-disubstituted furyl alcohols

Chan, Kin-Fai,Wong, Henry N. C.

, p. 3991 - 3994 (2007/10/03)

matrix presented The addition reactions of various nucleophiles to a furyl aldehyde bearing a chiral boronate at the C-3 position furnished chromatographically separable diastereomers. The R diastereoselection was more favorable when no additive was added

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