Cas 327977-95-7,(1S,2E)-1-(3-{[1-(tert-Butyl)-1,1-dimethylsilyl]oxy}propyl)-3-(phenylsulfonyl)prop-2-enyl acetate

327977-95-7

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Basic information

Product Name: (1S,2E)-1-(3-{[1-(tert-Butyl)-1,1-dimethylsilyl]oxy}propyl)-3-(phenylsulfonyl)prop-2-enyl acetate
Synonyms: (1S,2E)-1-(3-{[1-(tert-Butyl)-1,1-dimethylsilyl]oxy}propyl)-3-(phenylsulfonyl)prop-2-enyl acetate
CAS NO:327977-95-7
Molecular Formula:
Molecular Weight: 412.623
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,2E)-1-(3-{[1-(tert-Butyl)-1,1-dimethylsilyl]oxy}propyl)-3-(phenylsulfonyl)prop-2-enyl acetate(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2E)-1-(3-{[1-(tert-Butyl)-1,1-dimethylsilyl]oxy}propyl)-3-(phenylsulfonyl)prop-2-enyl acetate(327977-95-7)
EPA Substance Registry System: (1S,2E)-1-(3-{[1-(tert-Butyl)-1,1-dimethylsilyl]oxy}propyl)-3-(phenylsulfonyl)prop-2-enyl acetate(327977-95-7)

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: 327977-95-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 327977-95-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,7,9,7 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 327977-95:
(8*3)+(7*2)+(6*7)+(5*9)+(4*7)+(3*7)+(2*9)+(1*5)=197
197 % 10 = 7
So 327977-95-7 is a valid CAS Registry Number.

327977-95-7Upstream product

327977-95-7Downstream Products

327977-95-7Relevant academic research and scientific papers

Synthesis of enantioenriched substituted tetrahydrofurans and tetrahydropyrans via iron-mediated chirality transfer and ring closure

Enders,Nguyen

, p. 2092 - 2098 (2000)

The synthesis of optically active, functionalized tetrahydrofurans and tetrahydropyrans via Fe(CO)4-mediated cycloetherification has been accomplished. The ring closure reaction proceeds with chirality transfer and under retention of the configuration at the allylic carbon center.

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