Cas 207281-54-7,Methanesulfonic acid (1S,2S)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propyl ester

207281-54-7

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Basic information

Product Name: Methanesulfonic acid (1S,2S)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propyl ester
Synonyms: Methanesulfonic acid (1S,2S)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propyl ester
CAS NO:207281-54-7
Molecular Formula:
Molecular Weight: 503.692
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: Methanesulfonic acid (1S,2S)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Methanesulfonic acid (1S,2S)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propyl ester(207281-54-7)
EPA Substance Registry System: Methanesulfonic acid (1S,2S)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-phenyl-propyl ester(207281-54-7)

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: 207281-54-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 207281-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,2,8 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 207281-54:
(8*2)+(7*0)+(6*7)+(5*2)+(4*8)+(3*1)+(2*5)+(1*4)=117
117 % 10 = 7
So 207281-54-7 is a valid CAS Registry Number.

207281-54-7Upstream product

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207281-54-7Relevant academic research and scientific papers

A General, Catalytic, and Enantioselective Synthesis of (S)-γ-[(S)-1-Aminoalkyl]-γ-lactones

Aguilar, Núria,Moyano, Albert,Pericàs, Miquel A.,Riera, Antoni

, p. 3560 - 3567 (2007/10/03)

A catalytic asymmetric synthesis of N-phthaloyl (S)-γ-[(S)-1-aminoalkyl]-γ-lactones, widely used intermediates in the preparation of hydroxyethylene dipeptide isosteres, is described. The highly enantiopure epoxy alcohols arising from the Sharpless epoxid

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