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2-Oxazolidinone, 3-[(2R,3R)-1-[bis(trimethylsilyl)methyl]-2-(2-methylpropyl)-4-oxo-3-(phen ylmethyl)-3-azetidinyl]-4-phenyl-, (4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

651749-64-3

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651749-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651749-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,7,4 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 651749-64:
(8*6)+(7*5)+(6*1)+(5*7)+(4*4)+(3*9)+(2*6)+(1*4)=183
183 % 10 = 3
So 651749-64-3 is a valid CAS Registry Number.

651749-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R,4R)-3-benzyl-1-[bis(trimethylsilyl)methyl]-4-isobutyl-3-[(4S)-4-phenyl-2-oxo-oxazolidin-3-yl]-azetidin-2-one

1.2 Other means of identification

Product number -
Other names (S)-3-[(2R,3R)-3-Benzyl-1-(bis-trimethylsilanyl-methyl)-2-isobutyl-4-oxo-azetidin-3-yl]-4-phenyl-oxazolidin-2-one

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:651749-64-3 SDS

651749-64-3Relevant academic research and scientific papers

Synthesis of type II β-turn surrogate dipeptides based on syn-α-amino-α,β-dialkyl-β-lactams

Palomo, Claudio,Aizpurua, Jesus M.,Ganboa, Inaki,Benito, Ana,Cuerdo, Lourdes,Fratila, Raluca M.,Jimenez, Azucena,Loinaz, Iraida,Miranda, Jose I.,Pytlewska, Kinga R.,Micle, Andreea,Linden, Anthony

, p. 4443 - 4446 (2007/10/03)

(Chemical equation presented) The achiral bis(trimethylsilyl)methyl group acts as an efficient stereochemical determinant of the α-alkylation reaction in β-branched α-phenyloxazolidinyl- or α- diphenyloxazolidinyl-β-lactams and provides the first stereoco

Development of a New Family of Conformationally Restricted Peptides as Potent Nucleators of β-Turns. Design, Synthesis, Structure, and Biological Evaluation of β-Lactam Peptide Analogue of Melanostatin

Palomo, Claudio,Aizpurua, Jesus M.,Benito, Ana,Miranda, Jose Ignacio,Fratila, Raluca M.,Matute, Carlos,Domercq, Maria,Gago, Federico,Martin-Santamaria, Sonsoles,Linden, Anthony

, p. 16243 - 16260 (2007/10/03)

Novel enantiopure (i)-(β-lactam)-(Gly)-(i+3) peptide models, defined by the presence of a central α-alkyl-αamino-β-lactam ring placed as the (i+1) residue, have been synthesized in a totally stereocontrolled way by α-alkylation of suitable N-[bis(trimethy

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