Cas 960595-91-9,(2S,3R)-benzyl-[3-methyl-3-(4-methoxyphenoxy)-2-(2-nitrobenzenesulfonylamino)]-pent-4-ynoate

960595-91-9

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Basic information

Product Name: (2S,3R)-benzyl-[3-methyl-3-(4-methoxyphenoxy)-2-(2-nitrobenzenesulfonylamino)]-pent-4-ynoate
Synonyms: (2S,3R)-benzyl-[3-methyl-3-(4-methoxyphenoxy)-2-(2-nitrobenzenesulfonylamino)]-pent-4-ynoate
CAS NO:960595-91-9
Molecular Formula:
Molecular Weight: 524.551
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: (2S,3R)-benzyl-[3-methyl-3-(4-methoxyphenoxy)-2-(2-nitrobenzenesulfonylamino)]-pent-4-ynoate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R)-benzyl-[3-methyl-3-(4-methoxyphenoxy)-2-(2-nitrobenzenesulfonylamino)]-pent-4-ynoate(960595-91-9)
EPA Substance Registry System: (2S,3R)-benzyl-[3-methyl-3-(4-methoxyphenoxy)-2-(2-nitrobenzenesulfonylamino)]-pent-4-ynoate(960595-91-9)

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: 960595-91-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 960595-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,5,9 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 960595-91:
(8*9)+(7*6)+(6*0)+(5*5)+(4*9)+(3*5)+(2*9)+(1*1)=209
209 % 10 = 9
So 960595-91-9 is a valid CAS Registry Number.

960595-91-9Upstream product

960595-91-9Downstream Products

960595-91-9Relevant academic research and scientific papers

A regio- and stereoselective approach to quaternary centers from chiral trisubstituted aziridines

Forbeck, Erin M.,Evans, Cory D.,Gilleran, John A.,Li, Pixu,Joullie, Madeleine M.

, p. 14463 - 14469 (2008/09/17)

A thorough investigation of a regio- and stereospecific aziridine ring opening reaction presents new synthetic technology for the construction of a variety of quaternary β-substituted-α-amino functional groups. Mild, metal-free reaction conditions allow f

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