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Check Digit Verification of cas no

The CAS Registry Mumber 555153-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,5,1,5 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 555153-61:
(8*5)+(7*5)+(6*5)+(5*1)+(4*5)+(3*3)+(2*6)+(1*1)=152
152 % 10 = 2
So 555153-61-2 is a valid CAS Registry Number.

555153-61-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name	3-(benzyloxycarbonyl)-1-(tert-butoxycarbonyl)-3-(phenylselanyl)piperidin-2-one

1.2 Other means of identification

Product number	-
Other names	Benzyl 1-(tert-butoxycarbonyl)-2-oxo-3-(phenylseleno)piperidine-3-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:555153-61-2 SDS

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555153-61-2Relevant academic research and scientific papers

PIPERIDINYLHYDROXYETHYLPIPERIDINES AS MODULATORS OF CHEMOKINE RECEPTORS

-

Page/Page column 28-29, (2009/05/28)

The present invention relates to a compound of the formula (I), or a pharmaceutically acceptable salt thereof, wherein R1-R8 and X, m, and n are defined. Compounds and compositions of the present invention are useful the treatment of atherosclerosis.

Diastereoselective conjugate addition of organocuprates to chiral racemic olefinic amido esters. Formal total synthesis of paroxetine

Cossy, Janine,Mirguet, Olivier,Gomez Pardo, Domingo,Desmurs, Jean-Roger

, p. 475 - 482 (2007/10/03)

The diastereoselective conjugate addition of an organocopper reagent to a chiral racemic olefinic amido ester has been used as the key step in a formal total synthesis of paroxetine.

Synthesis of 3-Aminolactams as X-Gly Constrained Pseudodipeptides and Conformational Study of a Trp-Gly Surrogate

Ecija, Marta,Diez, Anna,Rubiralta, Mario,Casamitjana, Nuria,Kogan, Marcelo J.,Giralt, Ernest

, p. 9541 - 9553 (2007/10/03)

3-Amino-δ-valerolactams trans-11a-c were synthesized through conjugate addition and Curtius rearrangement and converted into Fmoc-{Trp-Gly}, Fmoc-{Ile-Gly}, and Fmoc-{Phe-Gly} pseudodipeptides. Conformational analyses of tripeptide analogues Ac-{Trp-Gly}-

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