Cas 199384-37-7,2-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-phenylselanyl-propionic acid tert-butyl ester

199384-37-7

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Basic information

Product Name: 2-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-phenylselanyl-propionic acid tert-butyl ester
Synonyms:
CAS NO:199384-37-7
Molecular Formula:
Molecular Weight: 385.362
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: 2-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-phenylselanyl-propionic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-phenylselanyl-propionic acid tert-butyl ester(199384-37-7)
EPA Substance Registry System: 2-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-phenylselanyl-propionic acid tert-butyl ester(199384-37-7)

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: 199384-37-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 199384-37-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,3,8 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 199384-37:
(8*1)+(7*9)+(6*9)+(5*3)+(4*8)+(3*4)+(2*3)+(1*7)=197
197 % 10 = 7
So 199384-37-7 is a valid CAS Registry Number.

199384-37-7Upstream product

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199384-37-7Relevant academic research and scientific papers

The Exocyclic Effect: Protecting Group Strategy to Enhance Stereoselectivity in Hydrogen Transfer Reactions of Acyclic Free Radicals

Guindon, Yvan,Faucher, Anne-Marie,Bourque, Elyse,Caron, Valerie,Jung, Grace,Landry, Serge R.

, p. 9276 - 9283 (2007/10/03)

To enhance the diastereoselectivity of the hydrogen transfer reaction of acyclic substrates bearing 1,2- or 1,3-diols, the feasibility of a strategy employing bifunctional protecting groups has been demonstrated. This strategy is based upon the "exocyclic

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