(1S,2S)-2-Fluorocyclopropanecarboxylic acid CAS 127199-14-8

(1S,2S)-2-Fluorocyclopropanecarboxylic acid CAS 127199-14-8

Identification

CAS Number

127199-14-8

Name

(1S,2S)-2-Fluorocyclopropanecarboxylic acid

Synonyms

(1S,2S)-2-Fluorcyclopropancarbonsäure [German] [ACD/IUPAC Name]
(1S,2S)-2-fluorocyclopropane-1-carboxylic acid
(1S,2S)-2-Fluorocyclopropanecarboxylic acid [ACD/IUPAC Name]
105919-34-4 [RN]
127199-14-8 [RN]
Acide (1S,2S)-2-fluorocyclopropanecarboxylique [French] [ACD/IUPAC Name]
cis-2-Fluoro-cyclopropanecarboxylic acid
Cis-2-fluorocyclopropanecarboxylic acid
Cyclopropanecarboxylic acid, 2-fluoro-, (1S,2S)- [ACD/Index Name]
MFCD19237459 [MDL number]
(1R,2S)-trans-2-Fluorocyclopropanecarboxylic acid
(1s,2s)-2-fluorocyclopropanecarboxylic acid(wx900028)
(1s,2s)-2-fluorocyclopropanecarboxylic acid??
(1S,2S)-2-fluorocyclopropanecarboxylicacid
(1S,2S)-rel-2-Fluorocyclopropanecarboxylic acid
(cis)-2-fluorocyclopropanecarboxylic acid
??(1s,2s)-2-fluorocyclopropanecarboxylic acid
127199-13-7 [RN]
cis-(1S,2S)-2-Fluorocyclopropanecarboxylic acid
cis-2-fluoro-cyclopropanecarboxylic acid(wx610334)
Cyclopropanecarboxylic acid, 2-fluoro-, (1S-cis)-
MFCD04972869
rac-(1R,2R)-2-fluorocyclopropane-1-carboxylic acid
Racemic cis-2-Fluorocyclopropanecarboxylic acid

SMILES

O=C(O)[C@@H]1C[C@@H]1F

StdInChI

InChI=1S/C4H5FO2/c5-3-1-2(3)4(6)7/h2-3H,1H2,(H,6,7)/t2-,3+/m1/s1

StdInChIKey

HZQKMZGKYVDMCT-GBXIJSLDSA-N

Molecular Formula

C4H5FO2

Molecular Weight

104.080

Properties

Appearance

White solid

Structure

structure of (1S,2S)-2-Fluorocyclopropanecarboxylic acid CAS 127199-14-8

Structure of (1S,2S)-2-Fluorocyclopropanecarboxylic acid CAS 127199-14-8

Safety Data

WGK Germany

3

MSDS Download

Specifications and Other Information of Our

Identification Methods

HNMR, HPLC

Purity

99% min

Water

≤1.0%

Maximum Individual Impurity

≤1.0%

Shelf Life

2 years

Storage

Store in room temperature for long time and dry place; in container tightly sealed; Protect from light.

Known Application

(1S,2S)-2-Fluorocyclopropanecarboxylic acid and its derivatives can act as chiral catalysts in asymmetric synthesis reactions. They can guide the reaction selectively to produce chiral products, thereby enhancing the stereo-selectivity and efficiency of the reaction.

Chiral compounds play a crucial role in the pharmaceutical industry as their chirality often correlates with their biological activity. (1S,2S)-2-Fluorocyclopropanecarboxylic acid and its derivatives may be employed in the synthesis of intermediates for chiral drugs or used as catalysts to control the stereo-selectivity during the synthesis process. (1S,2S)-2-Fluorocyclopropanecarboxylic acid can serve as a vital precursor in organic synthesis for generating various organic compounds with specific structures and properties. These compounds find applications in materials science fields such as optical materials, liquid crystal materials, and polymer materials.

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