Cas 889866-98-2,(S)-2-[(S)-2-(Pyrrolidine-1-carbonyl)-pyrrolidine-1-carbonyl]-pyrrolidine-1-carboxylic acid benzyl ester

889866-98-2

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Basic information

Product Name: (S)-2-[(S)-2-(Pyrrolidine-1-carbonyl)-pyrrolidine-1-carbonyl]-pyrrolidine-1-carboxylic acid benzyl ester
Synonyms: (S)-2-[(S)-2-(Pyrrolidine-1-carbonyl)-pyrrolidine-1-carbonyl]-pyrrolidine-1-carboxylic acid benzyl ester
CAS NO:889866-98-2
Molecular Formula:
Molecular Weight: 399.49
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: (S)-2-[(S)-2-(Pyrrolidine-1-carbonyl)-pyrrolidine-1-carbonyl]-pyrrolidine-1-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(S)-2-(Pyrrolidine-1-carbonyl)-pyrrolidine-1-carbonyl]-pyrrolidine-1-carboxylic acid benzyl ester(889866-98-2)
EPA Substance Registry System: (S)-2-[(S)-2-(Pyrrolidine-1-carbonyl)-pyrrolidine-1-carbonyl]-pyrrolidine-1-carboxylic acid benzyl ester(889866-98-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 889866-98-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 889866-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,9,8,6 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 889866-98:
(8*8)+(7*8)+(6*9)+(5*8)+(4*6)+(3*6)+(2*9)+(1*8)=282
282 % 10 = 2
So 889866-98-2 is a valid CAS Registry Number.

889866-98-2Upstream product

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889866-98-2Relevant academic research and scientific papers

A highly enantioselective organocatalyst for the Michael addition of cyclic ketones to nitroolefins

Zhu, Ming-Kui,Cun, Lin-Feng,Mi, Ai-Qiao,Jiang, Yao-Zhong,Gong, Liu-Zhu

, p. 491 - 493 (2006)

Enantiomerically pure triamine 2, which catalyses the Michael addition of cyclic ketones to nitroolefins with high diastereoselectivity (up to 99:1) and enantioselectivity (up to 91% ee), was designed and prepared.

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