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691011

Sigma-Aldrich

(S)-(−)-α-Allylalanine

≥98.0% (HPLC)

Synonym(s):

(S)-2-Amino-2-methyl-4-pentenoic acid

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About This Item

Empirical Formula (Hill Notation):
C6H11NO2
CAS Number:
96886-55-4
Molecular Weight:
129.16
MDL number:
MFCD00145248
UNSPSC Code:
12352200
eCl@ss:
32160406
PubChem Substance ID:
329761380
NACRES:
NA.22

assay

≥98.0% (HPLC)

form

powder

optical purity

ee: ≥98.0% (HPLC)

reaction suitability

reaction type: solution phase peptide synthesis

impurities

≤15% water

application(s)

peptide synthesis

storage temp.

2-8°C

SMILES string

C[C@](N)(CC=C)C(O)=O

InChI

1S/C6H11NO2/c1-3-4-6(2,7)5(8)9/h3H,1,4,7H2,2H3,(H,8,9)/t6-/m0/s1

InChI key

QMBTZYHBJFPEJB-LURJTMIESA-N

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Thanh K Pham et al.
Bioorganic chemistry, 101, 104024-104024 (2020-07-07)
The N-capping box is a distinct helix-stabilizing motif frequently found in proteins. In this study, we examined a ruthenium-mediated intramolecular backbone to side chain macrocyclization as a rigidified mimicry of the N-capping box. Experimental data indicate that the 15-membered macrocycle

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