(2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID

Product Name: (2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID
CAS No.: 176486-63-8
Chemical Name: (2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID
Synonyms: FMOC(2S,4R)-ABPC;RARECHEM EM WB 0068;FMOC-ABPC(2S,4R)-OH;BOC-L-PRO(4-NHFMOC)-OH;(4R)-1-Boc-4-(FMoc-aMino)-L-proline;N-BOC-TRANS-4-N-FMOC-AMINO-L-PROLINE;N-BOC-TRANS-4-(FMOC-AMINO)-L-PROLINE;(2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID;FMOC-(2S,4R)-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID;(2S,4R)-1-Boc-4-(Fmoc-amino)pyrrolidine-2-carboxylic Acid
CBNumber: CB3463329
Molecular Formula: C25H28N2O6
Formula Weight: 452.5
MOL File: 176486-63-8.mol

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(2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID Property

Melting point:: 199 °C(lit.)
Boiling point:: 650.2±55.0 °C(Predicted)
Density: 1.33
storage temp.: Keep in dark place,Sealed in dry,Room Temperature
pka: 3.81±0.40(Predicted)
form: Powder
color: White/off-white/palebrown
optical activity: [α]20/D 34°, c = 1 in chloroform

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Safety

Risk Statements: 22
Safety Statements: 36/37/38
WGK Germany: 3
HS Code: 29339900

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 534390
Product name: N-Boc-trans-4-N-Fmoc-amino-L-proline
Purity: 97%
Packaging: 1g
Price: $109.2
Updated: 2024/03/01

Alfa Aesar

Product number: H66878
Product name: N-Boc-trans-4-(Fmoc-amino)-L-proline, 97%
Packaging: 250mg
Price: $89.6
Updated: 2023/06/20

Alfa Aesar

Product number: H66878
Product name: N-Boc-trans-4-(Fmoc-amino)-L-proline, 97%
Packaging: 1g
Price: $267
Updated: 2023/06/20

TRC

Product number: B671300
Product name: N-Boc-trans-4-N-Fmoc-amino-L-proline
Packaging: 500mg
Price: $150
Updated: 2021/12/16

Matrix Scientific

Product number: 096999
Product name: (2S,4R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid
Purity: 95+%
Packaging: 250mg
Price: $115
Updated: 2021/12/16

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(2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID Chemical Properties,Usage,Production

Chemical Properties

solid

Uses

N-?Boc-?trans-?4-?N-?Fmoc-?amino-?L-?proline is used to prepare NS3-?serine protease inhibitors of hepatitis C virus.

(2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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(2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID Suppliers

China 74 Europe 1 France 2 Germany 3 India 2 Switzerland 2 United Kingdom 3 United States 14 Global 101

CHEMSTEP

Tel: --
Fax: --
Email: info@chemstep.com
Country: Europe
ProdList: 6143
Advantage: 51

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View Lastest Price from (2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID manufacturers

Honest Joy Holdings Limited

Product: Fmoc-ABPC(2S,4R)-OH 176486-63-8
Price: US $0.00/KG
Min. Order: 1KG
Purity: 97.4%
Supply Ability: 100 tons
Release date: 2022-01-17

176486-63-8, (2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACIDRelated Search:

BOC-L-Prolinol 1-Pyrrolidinecarboxylicacid,3-(methylamino)-,1,1-dimethylethylester,(R)-(9CI) Propamocarb tert-Butyl 3-aminopyrrolidine-1-carboxylate (2S,4R)-1-BOC-4-AMINO-PYRROLIDINE-2-CARBOXYLIC ACID (3R)-(+)-3-(METHYLAMINO)PYRROLIDINE (R)-(+)-1-Boc-3-aminopyrrolidine 1-Boc-3-Methylaminopyrrolidine L-Proline, 4-amino-, (4R)- (9CI) BOC-L-Proline (R)-3-Aminopyrrolidine tert-Butyl N-(3-aminopropyl)-N-methylcarbamate Boc-L-2,4-diaminobutyric acid N-Boc-D-proline (2S,4S)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID 1-Boc-Pyrrolidine ETHYL 3-AMINOPYRROLIDINE-1-CARBOXYLATE 1-BOC-AMINO-BUTYL-3-AMINE

(4R)-1-Boc-4-(FMoc-aMino)-L-proline

(2S,4R)-4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-1,2-Pyrrolidinedicarboxylic acid 1-(1,1-dimethylethyl) ester

(2S,4R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butoxycarbonyl)pyrrolidine-2-car

Fmoc-(2S,4R)-4-amino-1-Boc-pyrrolidine-2-carboxylic acid≥ 99% (HPLC)

RARECHEM EM WB 0068

N-BOC-TRANS-4-N-FMOC-AMINO-L-PROLINE

FMOC(2S,4R)-ABPC

FMOC-(2S,4R)-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID

FMOC-ABPC(2S,4R)-OH

BOC-L-PRO(4-NHFMOC)-OH

(2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID

(2S,4R)-N-(TERT-BUTOXYCARBONYL)-4-N-(9-FLUORENYLMETHOXYCARBONYL)AMINOPYRROLIDINE-2-CARBOXYLIC ACID

(2S,4R)-TRANS-N-ALPHA-TERT-BUTYLOXYCARBONYL-4-(9-FLUORENYLMETHYLOXYCARBONYL)AMINO-L-PROLINE

1,2-Pyrrolidinedicarboxylicacid,4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,1-(1,1-dimethylethyl)ester,(2S,4R)-(9CI)

N-BOC-TRANS-4-(FMOC-AMINO)-L-PROLINE

(2S,4R)-trans-N-alpha-t-Butyloxycarbonyl-4-(9-fluorenylmethyloxycarbonyl)amino-L-proline

(2R,4R)-4-(((9H-fluoren-9-yl)methoxy)carbonylamino)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid

(2S,4R)-4-(((9H-fluoren-9-yl)methoxy)carbonylamino)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid

(2R,4R)-4-(((9H-fluoren-9-yl)Methoxy)carbonylaMino)-1-(tert-buto

(2S,4R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butoxycarbonyl)pyrrolidine-2-carbox

(2S,4R)-4-Aminopyrrolidine-2-carboxylic acid, N1-BOC 4-FMOC protected

trans-4-Amino-L-proline, N1-BOC 4-FMOC protected, (4R)-1-(tert-Butoxycarbonyl)-4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-L-proline

(2S,4R)-4-(((9H-fluoren-9-yl)Methoxy)carbonylaMino)-1-(tert-butoxycarbonyl)pyrolidine-2-carboxylic acid

(2S,4R)-1-[(tert-butoxy)carbonyl]-4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pyrrolidine-2-carboxylic acid

1,2-Pyrrolidinedicarboxylic acid, 4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, 1-(1,1-dimethylethyl) ester, (2S,4R)-

(2S,4R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylicaci

(2S,4R)-FMOC-4-AMINO-1-BOC-PYRROLIDINE-2-CARBOXYLIC ACID USP/EP/BP

(2S,4R)-1-Boc-4-(Fmoc-amino)pyrrolidine-2-carboxylic Acid

176486-63-8

17486-63-8

Peptide Synthesis

Proline Derivatives

Specialty Synthesis

Unnatural Amino Acid Derivatives

FMOC