ChemicalBook > Product Catalog >Biochemical Engineering >Amino Acids and Derivatives >BOC-amino acid >(+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID

(+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID

(+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID Structure
CAS No.
151907-80-1
Chemical Name:
(+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID
Synonyms
Boc-L-PEC;BOC-L-ACPEC;Peramivir impurities9;(+)-(1R,4S)-Boc-g-Homocycloleu-2-ene;(+)-(1R,4S)-Boc-g-Homocycloleu-2-ene;(+)-(1R,4S)-N-Boc-g-homocycloleu-2-ene;(+)-(1R,4S)-N-BOC-GAMMA-HOMOCYCLOLEU-2-ENE;(1R,4S)-Boc-4-aminocyclopent-2-ene-carboxylic acid;(1R,4S)-4-Boc-aMino-cyclopent-2-enecarboxylic acid;(1R,4S)-4-(Boc-amino)-2-cyclopentenecarboxylic Acid
CBNumber:
CB5723368
Molecular Formula:
C11H17NO4
Molecular Weight:
227.26
MOL File:
151907-80-1.mol
MSDS File:
SDS
Modify Date:
2023/4/23 13:52:06

(+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID Properties

Melting point 152°C
Boiling point 382.3±42.0 °C(Predicted)
Density 1.18
storage temp. 2-8°C
pka 4.31±0.40(Predicted)
form Crystalline Powder
color Off-white
optical activity [α]20/D +48.5±2°, c = 1% in methanol
BRN 6177417
InChIKey WOUNTSATDZJBLP-JGVFFNPUSA-N

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
10-23
HazardClass  IRRITANT
HS Code  29223900

(+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID Chemical Properties,Uses,Production

Chemical Properties

off-white crystalline powder

(+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 148)Suppliers
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(+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID Spectrum

(1R,4S)-(+)-4-(BOC-AMINO)-2-CYCLOPENTENE-1-CARBOXYLIC ACID (+)-(1R,4S)-N-T-BUTOXYCARBONYL-1-AMINOCYCLOPENT-2-ENE-4-CARBOXYLIC ACID (1R,4S)-(-)-4-AMINOCYCLOPENT-2-ENE-1-CARBOXYLIC ACID, N-BOC PROTECTED (1R,4S)-(-)-4-(TERT-BUTOXYCARBONYL)AMINOCYCLOPENT-2-ENE-1-CARBOXYLIC ACID (+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENE-4-CARBOXYLIC ACID (+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID (+)-(1R,4S)-N-BOC-GAMMA-HOMOCYCLOLEU-2-ENE (+)-(1S,4R)-N-BOC-1-AMINOCYCLOPENT-2-ENE-4-CARBOXYLIC ACID (1S,4R)-N-BOC-1-AMINOCYCLOPENT-2-ENE-4-CARBOXYLIC ACID (1S,4R)-N-TERT-BUTOXYCARBONYL-1-AMINO-2-CYCLOPENTENE-4-CARBOXYLIC ACID (1R,4S)-(+)-4-(BOC-AMINO)-2-CYCLOPENTENE -1-CARBOXYLIC ACID 98+% (+)-(1R,4S)-N-Boc-g-homocycloleu-2-ene (1S,4R)-N-BOC-1-Aminocyclopent-2-ene-4-carboxylic acid, 98% ee (1R,4S)-Boc-4-aminocyclopent-2-ene-carboxylic acid (1R,4S)-4-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-cyclopentene-1-carboxylic acid (1R,4S)-4-Boc-aMino-cyclopent-2-enecarboxylic acid (+)-(1R,4S)-N-Butoxycarbonyl-4-aMinocyclopent-2-enecarboxylic acid BOC-L-ACPEC (1R,4S)-(+)-4-(Boc-aMino)-2-cyclopentene-1-carboxylic acid Cis-(1R,4S)-4-Boc-aMino-2-Cyclopentene-1-carboxylic acid (1R,4S)-4-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-1-cyclopent-2-enecarboxylic acid cis-N-tert-Butoxycarbonyl-4-aminocyclopent-2-ene-1-carboxylic acid (+)-(1R,4S)-N-(Tert-Butoxy)Carbonyl 4-Aminocyclopent-2-enecarboxylic acid (+)-(1R,4S)-Boc-g-Homocycloleu-2-ene (1R,4S)-4-{[(2,2-dimethylpropanoyl)oxy]amino}cyclopent-2-ene-1-carboxylic acid (1R,4S)-4-tert-Boc-amino-cyclopent-2-enecarboxylic acid 4S)-(+)-4-(BOC-AMINO)-2-CYCLOPENTENE-1-CARBOXYLIC ACID 4S)-N-T-BUTOXYCARBONYL-1-AMINOCYCLOPENT-2-ENE-4-CARBOXYLIC ACID Boc-L-PEC 2-Cyclopentene-1-carboxylic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-, (1R,4S)- (1S,4R)-N-BOC-1-Aminocyclopent-2-ene-4-carboxylicaci (+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID USP/EP/BP (+)-(1R,4S)-4-[(t-Butoxycarbonyl)amino]cyclopent-2-ene-1-carboxylic acid Peramivir impurities9 (+)-(1R,4S)-Boc-g-Homocycloleu-2-ene (+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID (1R,4S)-4-(Boc-amino)-2-cyclopentenecarboxylic Acid 151907-80-1 Alicyclic Amino Acids Peptide Synthesis Specialty Synthesis Unnatural Amino Acid Derivatives Unusual amino acids Alicyclic Amino Acids Peptide Synthesis Unnatural Amino Acid Derivatives