Cas 1356485-59-0,(R)-1-((2S,3S)-3-(benzylamino)-4,6-dimethoxy-2,3-dihydrobenzofuran-2-yl)-2-(tert-butyldimethylsilyloxy)ethanol

1356485-59-0

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Basic information

Product Name: (R)-1-((2S,3S)-3-(benzylamino)-4,6-dimethoxy-2,3-dihydrobenzofuran-2-yl)-2-(tert-butyldimethylsilyloxy)ethanol
Synonyms:
CAS NO:1356485-59-0
Molecular Formula:
Molecular Weight: 459.658
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: (R)-1-((2S,3S)-3-(benzylamino)-4,6-dimethoxy-2,3-dihydrobenzofuran-2-yl)-2-(tert-butyldimethylsilyloxy)ethanol(CAS DataBase Reference)
NIST Chemistry Reference: (R)-1-((2S,3S)-3-(benzylamino)-4,6-dimethoxy-2,3-dihydrobenzofuran-2-yl)-2-(tert-butyldimethylsilyloxy)ethanol(1356485-59-0)
EPA Substance Registry System: (R)-1-((2S,3S)-3-(benzylamino)-4,6-dimethoxy-2,3-dihydrobenzofuran-2-yl)-2-(tert-butyldimethylsilyloxy)ethanol(1356485-59-0)

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: 1356485-59-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1356485-59-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,6,4,8 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1356485-59:
(9*1)+(8*3)+(7*5)+(6*6)+(5*4)+(4*8)+(3*5)+(2*5)+(1*9)=190
190 % 10 = 0
So 1356485-59-0 is a valid CAS Registry Number.

1356485-59-0Upstream product

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1356485-59-0Relevant academic research and scientific papers

Taming the friedel-crafts reaction: Organocatalytic approach to optically active 2,3-dihydrobenzofurans

Albrecht, Lukasz,Ransborg, Lars Krogager,Lauridsen, Vibeke,Overgaard, Mette,Zweifel, Theo,Jorgensen, Karl Anker

, p. 12496 - 12500 (2012/01/15)

Fine-tuning: Three types of optically active trans-2,3-disubstituted-2,3- dihydrobenzofurans having three contiguous stereogenic centers can be efficiently accessed by one-pot reaction cascades (see scheme; TMS=trimethylsilyl). High substitution diversity of the final products can be achieved from the same common precursors by fine-tuning of their reactivity through simple structural modifications. Copyright

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