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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

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

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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