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Boc-cis-L-4-Fluoroproline

(2S,4S)-4-Fluoro-N-Boc-Pyrrolidine-2-carboxylic acid

CAS: 203866-13-1

Molecular Formula: C10H16FNO4

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Boc-cis-L-4-Fluoroproline - Names and Identifiers

Name (2S,4S)-4-Fluoro-N-Boc-Pyrrolidine-2-carboxylic acid
Synonyms Boc-cis-4-fluoro-Pro-OH
Boc-cis-L-4-Fluoroproline
N-BOC-cis-4-fluoro-L-proline
N-t-BOC-cis-4-Fluoro-L-proline
(2S,4S)-N-Boc-cis-4-Fluoro-L-proline
cis-4-Fluoro-L-proline, N-BOC protected
(4S)-1-(tert-butoxycarbonyl)-4-fluoro-L-proline
(2S,4S)-Boc-4-fluoro-pyrrolidine-2-carboxylic acid
(2S,4S)-N-Boc-4-fluoropyrrolidine-2-carboxy lic acid
(2S,4S)-4-Fluoro-N-Boc-Pyrrolidine-2-carboxylic acid
Boc-(2S,4S)-4-fluoro-pyrrolidine-2-carboxylic acid, Boc-flp-OH
(2S,4S)-4-Fluoropyrrolidine-2-carboxylic acid, N-BOC protected
4S)-1-(tert-Butoxycarbonyl)-4-fluoro-2-pyrrolidinecarboxylic Acid
(2S,4S)-4-Fluoro-1-tert-butoxycarbonyl-pyrrolidine-2-carboxylic acid
(2S,4S)-1-Boc-4-fluoro-2-pyrrolidinecarboxylic Acid N-(tert-Butoxycarbonyl)-cis-4-fluoro-L-proline N-Boc-cis-4-fluoro-L-proline
CAS 203866-13-1
InChI InChI=1/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-/m0/s1
InChIKey YGWZXQOYEBWUTH-BQBZGAKWSA-N

Boc-cis-L-4-Fluoroproline - Physico-chemical Properties

Molecular FormulaC10H16FNO4
Molar Mass233.24
Density1.24±0.1 g/cm3(Predicted)
Melting Point157-161.°C
Boling Point346.0±42.0 °C(Predicted)
Flash Point163°C
Vapor Presure1.05E-05mmHg at 25°C
AppearanceSolid
pKa3.53±0.40(Predicted)
Storage ConditionKeep in dark place,Sealed in dry,Room Temperature
Refractive Index-57 ° (C=1, MeOH)
MDLMFCD04973957

Boc-cis-L-4-Fluoroproline - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany3
HS Code29339900
Hazard ClassIRRITANT

Boc-cis-L-4-Fluoroproline - Reference Information

introduction (2S,4S)-N-Boc-cis -4-fluorine-L-proline is solid at normal temperature and pressure,(2S,4S)-N-Boc-cis -4-fluorine-L-proline is an amino acid derivative of proline series, it is widely used in the synthesis of biological macromolecules and bioactive molecules.
use (2S,4S)-N-Boc-cis -4-fluorine-L-proline is an amino acid derivative of proline series and has a wide range of applications in the synthesis of biological macromolecules. In the synthetic transformation, the carboxyl group in the structure can become a hydroxyl group under the reduction of borane, and the Boc group is not affected during the reduction process; in addition, the carboxyl group can also be converted into an amide group.
preparation method
at room temperature, to 2-methyl (2S,4S)-4-fluoropyrrolidine -1, 2-dicarboxylic acid tert-butyl ester (2.46g, 9.96 mmol) 10ml of water was added to a solution of dioxane (20 ml), then lithium hydroxide hydrate (2.09g, 49.8 mmol) was added slowly, and the resulting mixture was reacted with stirring for 3 hours (monitored by TLC). After the reaction is over, filter the solution to remove insoluble substances, evaporate the obtained filtrate in vacuum to remove the solvent, add the residue to 10mL of water, acidify the residue to pH 3-4 with concentrated hydrochloric acid, and slowly precipitate, filter and dry the solid precipitate to obtain the target product (2S,4S)-N-Boc-cis -4-fluorine-L-proline.

Figure (2S,4S)-Synthesis route of N-Boc-cis-4-fluoro-L-proline
Last Update:2024-04-09 01:59:58
Boc-cis-L-4-Fluoroproline
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View History
Boc-cis-L-4-Fluoroproline
6ALPHA-DEOXY-6ALPHA-AZIDO-4ALPHA-DEOXY-4ALPHA-(THYMIN-1-YL)-2,3ALPHA:2ALPHA,5ALPHA-DIANHYDRO-L-ALTROFURANOSE DIMETHYL ACETAL
6-氯-3-氰基邻二氮杂苯
N-(tert-Butyloxycarbonyl)glutamic acid 5-tert-butyl ester
TRANS-O-METHYL-O-COUMARIC ACID
direct fast brown
2,4-DIBROMO-6-NITROANILINE
cis-3-Aminocyclohexanecarboxylic Acid
α-高野尻霉素
双(二苄基丙酮)钯
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