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Key Documents

687332

Sigma-Aldrich

N-Boc-trans-4-fluoro-L-proline

97%

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About This Item

Empirical Formula (Hill Notation):
C10H16FNO4
CAS Number:
Molecular Weight:
233.24
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

97%

form

solid

optical activity

[α]22/D -65.0±5°, c = 1 in chloroform

mp

115-119 °C

functional group

carboxylic acid
fluoro

SMILES string

CC(C)(C)OC(=O)N1C[C@H](F)C[C@H]1C(O)=O

InChI

1S/C10H16FNO4/c1-10(2,3)16-9(15)12-5-6(11)4-7(12)8(13)14/h6-7H,4-5H2,1-3H3,(H,13,14)/t6-,7+/m1/s1

InChI key

YGWZXQOYEBWUTH-RQJHMYQMSA-N

Application

N-Boc-trans-4-fluoro-L-proline can be used in the preparation of benzophenone based ligand, which is further used to synthesize Ni(II) Schiff base complex.

pictograms

Exclamation mark

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

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Synthesis, Ni (II) Schiff base complexation and structural analysis of fluorinated analogs of the ligand (S)-2-[N-(N′-benzylprolyl) amino] benzophenone (BPB)
Tatum NJ, et al.
Journal of Fluorine Chemistry, 173, 77-83 (2015)

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