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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

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

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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