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06486

Sigma-Aldrich

Boc-(S)-α-allyl-Pro-OH

≥98.0%

Synonym(s):

(S)-2-Allyl-1-Boc-2-pyrrolidinecarboxylic acid, Boc-α-allyl-D-proline

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About This Item

Empirical Formula (Hill Notation):
C13H21NO4
CAS Number:
Molecular Weight:
255.31
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥98.0%

form

powder

reaction suitability

reaction type: Boc solid-phase peptide synthesis

color

white to off-white

mp

120-122 °C

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N1CCC[C@]1(CC=C)C(O)=O

InChI

1S/C13H21NO4/c1-5-7-13(10(15)16)8-6-9-14(13)11(17)18-12(2,3)4/h5H,1,6-9H2,2-4H3,(H,15,16)/t13-/m1/s1

InChI key

ZTMLHNDSVVOEEH-CYBMUJFWSA-N

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral

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

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Articles

Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.

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