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26250-90-8

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26250-90-8 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 26250-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,5 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26250-90:
(7*2)+(6*6)+(5*2)+(4*5)+(3*0)+(2*9)+(1*0)=98
98 % 10 = 8
So 26250-90-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H21NO4/c1-15(2,3)20-14(19)16-10-12(13(17)18)9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/m1/s1

26250-90-8 Well-known Company Product Price

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  • Aldrich

  • (670243)  rac-Boc-β2-homophenylalanine  ≥96% (HPLC)

  • 26250-90-8

  • 670243-500MG

  • 2,589.21CNY

  • Detail

26250-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (R,S)-Boc-3-amino-2-benzyl-propionic acid

1.2 Other means of identification

Product number -
Other names N-Boc-3-amino-2-benzylpropionic acid

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:26250-90-8 SDS

26250-90-8Downstream Products

26250-90-8Relevant articles and documents

Catalytic Asymmetric Synthesis of Unprotected β2-Amino Acids

Zhu, Chendan,Mandrelli, Francesca,Zhou, Hui,Maji, Rajat,List, Benjamin

, p. 3312 - 3317 (2021/04/07)

We report here a scalable, catalytic one-pot approach to enantiopure and unmodified β2-amino acids. A newly developed confined imidodiphosphorimidate (IDPi) catalyzes a broadly applicable reaction of diverse bis-silyl ketene acetals with a silylated aminomethyl ether, followed by hydrolytic workup, to give free β2-amino acids in high yields, purity, and enantioselectivity. Importantly, both aromatic and aliphatic β2-amino acids can be obtained using this method. Mechanistic studies are consistent with the aminomethylation to proceed via silylium-based asymmetric counteranion-directed catalysis (Si-ACDC) and a transition state to explain the enantioselectivity is suggested on the basis of density functional theory calculation.

Beta amino acid-modified and fluorescently labelled kisspeptin analogues with potent KISS1R activity

Camerino,Liu,Moriya,Kitahashi,Mahgoub,Mountford,Chalmers,Soga,Parhar,Thompson

, p. 406 - 414 (2016/08/28)

Kisspeptin analogues with improved metabolic stability may represent important ligands in the study of the kisspeptin/KISS1R system and have therapeutic potential. In this paper we assess the activity of known and novel kisspeptin analogues utilising a du

Organocatalysed decarboxylative protonation process from Meldrum's acid: Enantioselective synthesis of isoxazolidinones

Tite, Tony,Sabbah, Mohamad,Levacher, Vincent,Briere, Jean-Francois

, p. 11569 - 11571 (2013/12/04)

An asymmetric organocatalysed decarboxylative protonation reaction allowed a straightforward synthesis of α-substituted isoxazolidin-5-ones from readily available 5-substituted Meldrum's acids. This process is initiated by an anionic formal (3+2) cycloaddition-fragmentation, generated in-situ from a sulfone-amide precursor which also served as a latent source of proton.

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