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1-(Boc-amino)cyclopropanecarboxylic acid

1-(Boc-amino)cyclopropanecarboxylic acid Structure
CAS No.
88950-64-5
Chemical Name:
1-(Boc-amino)cyclopropanecarboxylic acid
Synonyms
Boc-ACC-OH;BOC-AC3C-OH;BOC-ACPC-OH;BOC-1, 1-ACCP;Boc-1-aminocycL;BOC-(1)NH-DELTA-OH;BOC-(1)NHCPROPN-OH;RARECHEM AR PA 0007;1-{[(tert-butoxy)carbonyl]amino};Boc-1-aminocyclopropyl formic acid
CBNumber:
CB0409746
Molecular Formula:
C9H15NO4
Molecular Weight:
201.22
MOL File:
88950-64-5.mol
Modify Date:
2024/4/24 17:21:39

1-(Boc-amino)cyclopropanecarboxylic acid Properties

Melting point 178 °C
Boiling point 347.6±21.0 °C(Predicted)
Density 1.21±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
pka 4.04±0.20(Predicted)
form Solid
color White to Off-White
BRN 4430628
InChI InChI=1S/C9H15NO4/c1-8(2,3)14-7(13)10-9(4-5-9)6(11)12/h4-5H2,1-3H3,(H,10,13)(H,11,12)
InChIKey DSKCOVBHIFAJRI-UHFFFAOYSA-N
SMILES C1(NC(OC(C)(C)C)=O)(C(O)=O)CC1
CAS DataBase Reference 88950-64-5(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P271-P280
Hazard Codes  Xi,Xn,O
Risk Statements  36/37/38-22
Safety Statements  26-36-36/37/39-22
WGK Germany  3
HazardClass  IRRITANT
HS Code  29242990
NFPA 704
0
2 0

1-(Boc-amino)cyclopropanecarboxylic acid price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 39977 1-(Boc-amino)cyclopropanecarboxylic acid ≥98.0% (TLC) 88950-64-5 1G ₹27094.98 2022-06-14 Buy
Product number Packaging Price Buy
39977 1G ₹27094.98 Buy

1-(Boc-amino)cyclopropanecarboxylic acid Chemical Properties,Uses,Production

Description

1-(Boc-amino)cyclopropanecarboxylic acid is an important organic compound. It is used in the biological field for the synthesis of irreversible inhibitors of tetrapeptide carboxypeptidases, leading to covalent substrate modifications; preparation of combinatorial libraries. It is used in the synthetic field as a pharmaceutical synthesis intermediate.

Chemical Properties

White crystalline powder

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1-(Boc-amino)cyclopropanecarboxylic acid Spectrum

BOC-ACPC-OH BOC-AC3C-OH BOC-(1)NHCPROPN-OH BOC-(1)NH-DELTA-OH BOC-1-AMINOCYCLOPROPANE-1-CARBOXYLIC ACID BOC-1-AMINO-1-CYCLOPROPANE CARBOXYLIC ACID BOC-1, 1-ACCP 1-(BOC-AMINO)CYCLOPROPANECARBOXYLIC ACID 1-(N-T-BOC-AMINO)-CYCLOPROPANECARBOXYLIC ACID 1-N-(BOC)AMINO-CYCLOPROPANE-1-CARBOXYLIC ACID 1-(TERT-BUTYLOXYCARBONYL-AMINO)-CYCLOPROPYL-1-CARBOXYLIC ACID 1-[(TERT-BUTOXYCARBONYL)AMINO]CYCLOPROPANECARBOXYLIC ACID N-ALPHA-T-BUTOXYCARBONYL-1-AMINO-CYCLOPROPANE-1-CARBOXYLIC ACID N-ALPHA-T-BUTOXYCARBONYL-1-AMINO-CYCLOPROPANECARBOXYLIC ACID RARECHEM AR PA 0007 1-(Boc-amino)cyclopropanecarboxylic acid 1-[(tert-Butoxycarbonyl)amino]cyclopropanecarboxylic acid Boc-1-aminocyclopropane-1-carboxylic acid≥ 99% (HPLC) Boc-1-Aminocyclopropanecarboxylic acid 1-[(BOC)AMINO] CYCLOPANECARBOXYLIC ACID 1-[(tert-Butoxycarbonyl)amino]cyclopropanecarboxylic acid 97% 1-(T-BUTYLOXYCARBONYL-AMINO)-CYCLOPROPYL-1-CARBOXYLIC ACID 1-(TERT-BOC-AMINO)CYCLOPROPANECARBOXYLIC ACID N-Boc-1-aminocyclopropanecarboxylic acid 1-[(tert-Butoxycarbonyl)amino]cyclopropane-1-carboxylic acid 1-Aminocyclopropane-1-carboxylic acid, N-BOC protected Boc-ACC-OH 1-(N-tert-butoxycarbonyl-amino)cyclopropanecarboxylic acid 1-Aminocyclopropane-1-carboxylic acid, N-BOC protected 97% 1-(tert-butoxycarbonyl)cyclopropanecarboxylic acid Boc-ACPC-OH Boc-1-AMinocyclopropane-1-carboxylic acid 1-(Boc-amino)cyclopropanecarboxylic acid ,98% 1-[(tert-Butoxycarbonyl)amino]cyclopropane-1-carboxylic acid, 1-[(tert-Butoxycarbonyl)amino]-1-carboxycyclopropane N-t-BOC-1-AMino-1-cyclopropanecarboxylic acid Boc-1-aminocycL Cyclopropanecarboxylic acid, 1-[[(1,1-dimethylethoxy)carbonyl]amino]- Boc-1-aminocyclopropyl formic acid 1-(Boc-amino)cyclopropanecarboxylic acid USP/EP/BP 1-<(tert-butyloxy)carbonylamino>cyclopropane-1-carboxylic acid 1-[(2-methylpropan-2-yl)oxycarbonylamino]cyclopropane-1-carboxylic acid 1-{[(tert-butoxy)carbonyl]amino} 88950-64-5 88950-64-2 C9H15NO4 Unnatural Amino Acid Derivatives Peptide Synthesis Alicyclic Amino Acids Specialty Synthesis Alicyclic Amino Acids Peptide Synthesis Unnatural Amino Acid Derivatives Peptide Carboxylic Acids Ring Systems Amino Acids and Derivatives Carboxylic Acids Amino Acid Derivatives