ChemicalBook >> CAS DataBase List >>(+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID

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

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
MDL Number:
MFCD00211288
MOL File:
151907-80-1.mol
MSDS File:
SDS
Last updated:2023-04-23 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)  GHS hazard pictograms
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 price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B603255 (+)-(1R,4S)-N-Boc-4-aminocyclopent-2-enecarboxylicAcid 151907-80-1 500mg $100 2021-12-16 Buy
TRC B603255 (+)-(1R,4S)-N-Boc-4-aminocyclopent-2-enecarboxylicAcid 151907-80-1 100mg $45 2021-12-16 Buy
Matrix Scientific 041320 (1R,4S)-Boc-4-aminocyclopent-2-ene-carboxylic acid 151907-80-1 250mg $164 2021-12-16 Buy
Apolloscientific OR5860 (1R,4S)-(-)-4-Aminocyclopent-2-ene-1-carboxylicacid,N-BOCprotected 151907-80-1 5g $267 2021-12-16 Buy
Biosynth Carbosynth FB44068 (1R,4S)-4-((tert-Butoxycarbonyl)amino)cyclopent-2-enecarboxylic acid 151907-80-1 1g $285 2021-12-16 Buy
Product number Packaging Price Buy
B603255 500mg $100 Buy
B603255 100mg $45 Buy
041320 250mg $164 Buy
OR5860 5g $267 Buy
FB44068 1g $285 Buy

(+)-(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( 147)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
Shanghai UCHEM Inc.
+862156762820 +86-13564624040 sales@myuchem.com China 6711 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29321 58
Alfa Chemistry
info@alfa-chemistry.com United States 2344 58
SpiroChem AG
contact@spirochem.com United States 38 58

View Lastest Price from (+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID pictures 2021-01-06 (+)-(1R,4S)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID
151907-80-1
US $17.00 / g 1g 95% 1KG Career Henan Chemica Co

(+)-(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