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4-Pentenoic acid, 2-[(9-phenyl-9H-fluoren-9-yl)amino]-, 1,1-dimethylethyl ester, (2R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

659726-44-0

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659726-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 659726-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,9,7,2 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 659726-44:
(8*6)+(7*5)+(6*9)+(5*7)+(4*2)+(3*6)+(2*4)+(1*4)=210
210 % 10 = 0
So 659726-44-0 is a valid CAS Registry Number.

659726-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name t-butyl (R)-N-(9-phenyl-9H-fluoren-9-yl)allylglycinate

1.2 Other means of identification

Product number -
Other names (R)-2-(9-Phenyl-9H-fluoren-9-ylamino)-pent-4-enoic acid tert-butyl ester

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:659726-44-0 SDS

659726-44-0Downstream Products

659726-44-0Relevant articles and documents

Iminoiodane mediated aziridination of α-allylglycine: Access to a novel rigid arginine derivative and to the natural amino acid enduracididine

Sanière, Laurent,Leman, Lo?c,Bourguignon, Jean-Jacques,Dauban, Philippe,Dodd, Robert H.

, p. 5889 - 5897 (2007/10/03)

The synthesis of fully protected aminodihydrohistidines in optically pure form is described starting from allylglycine derivatives. These compounds represent novel conformationally constrained analogues of arginine, one of them being, in addition, a protected form of the marine natural product, enduracididine. The key step of the strategy is a one-pot copper-catalyzed aziridination of t-butyl (S)-N-(9-phenyl-9H-fluoren-9-yl)allylglycinate ((S)-16) with 2-trimethylsilylethanesulfonamide in the presence of iodosylbenzene.

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