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1-(Boc-amino)cyclopropanecarboxylic acid

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
MDL Number:
MFCD00083257
MOL File:
88950-64-5.mol
MSDS File:
SDS
Last updated:2026-01-13 11:13:03
Product description Number Pack Size Price
1-(Boc-amino)cyclopropanecarboxylic acid ≥98.0% (TLC) 39977 1g $572
1-[(tert-Butoxycarbonyl)amino]cyclopropanecarboxylic Acid min. 95.0 % B3138 5G $127
1-[(tert-Butoxycarbonyl)amino]cyclopropanecarboxylic Acid min. 95.0 % B3138 25G $380
1-(Boc-amino)cyclopropanecarboxylic acid B619645 5G $200
Boc-1-aminocyclopropane-1-carboxylic acid 266539 500mg $333
More product size

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
Major Application peptide synthesis
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)
UNSPSC Code 12352106

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P271-P280
PPE Eyeshields, Gloves, type N95 (US)
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
Storage Class 11 - Combustible Solids
NFPA 704
0
2 0

1-(Boc-amino)cyclopropanecarboxylic acid price More Price(50)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 39977 1-(Boc-amino)cyclopropanecarboxylic acid ≥98.0% (TLC) 88950-64-5 1g $572 2023-06-20 Buy
TCI Chemical B3138 1-[(tert-Butoxycarbonyl)amino]cyclopropanecarboxylic Acid min. 95.0 % 88950-64-5 5G $127 2026-03-19 Buy
TCI Chemical B3138 1-[(tert-Butoxycarbonyl)amino]cyclopropanecarboxylic Acid min. 95.0 % 88950-64-5 25G $380 2026-03-19 Buy
TRC B619645 1-(Boc-amino)cyclopropanecarboxylic acid 88950-64-5 5G $200 2021-12-16 Buy
Usbiological 266539 Boc-1-aminocyclopropane-1-carboxylic acid 88950-64-5 500mg $333 2021-12-16 Buy
Product number Packaging Price Buy
39977 1g $572 Buy
B3138 5G $127 Buy
B3138 25G $380 Buy
B619645 5G $200 Buy
266539 500mg $333 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

Uses

1-(Boc-amino)cyclopropanecarboxylic Acid is used as a reagent in the synthesis of pyrrolotriazinone derivatives as therapeutic PI3K inhibitors. Also used as a reagent in the synthesis of ether, carbamate and ester derivatives of adarotene as potential antitumor agents.

reaction suitability

reaction type: Boc solid-phase peptide synthesis

Synthesis

Di-tert-butyl dicarbonate

24424-99-5

1-Aminocyclopropane-1-carboxylic acid hydrochloride

68781-13-5

1-(Boc-amino)cyclopropanecarboxylic acid

88950-64-5

General procedure for the synthesis of Boc-1-aminocyclopropanecarboxylic acid from di-tert-butyl dicarbonate and 1-aminocyclopropanecarboxylic acid hydrochloride: 4.18 g (30.37 mmol) of 1-aminocyclopropanecarboxylic acid hydrochloride was dissolved in 61 ml of dichloromethane and 4.7 ml (33.40 mmol) of triethylamine (TEA) was added. The mixture was stirred for 10 minutes and then the dichloromethane was removed by evaporation under reduced pressure. The reaction was dissolved in a solvent mixture of 36.5 ml of 1N NaOH solution and 101 ml of 1,4-dioxane, followed by the addition of 8.4 ml (36.44 mmol) of di-tert-butyl dicarbonate (Boc2O). The reaction mixture was stirred at room temperature for 16 h, after which the 1,4-dioxane was removed by evaporation under reduced pressure. The residue was acidified to pH 3 with 1N HCl and then extracted with 3100 ml of ethyl acetate. The organic phase was dried with anhydrous magnesium sulfate and after evaporation of the solvent under reduced pressure, 3.59 g of 1-(tert-butoxycarbonylamino)cyclopropylacetic acid was obtained in 59% yield. The product was characterized by 1H NMR (400 MHz, MeOD): δ 1.51 (s, 2H), 1.51 (s, 9H), 1.44 (s, 4H).

References

[1] Patent: EP2865664, 2015, A1. Location in patent: Paragraph 0088; 0089
[2] Tetrahedron, 2013, vol. 69, # 16, p. 3495 - 3505

24424-99-5
22059-21-8
88950-64-5
Synthesis of 1-(Boc-amino)cyclopropanecarboxylic acid from Di-tert-butyl dicarbonate and 1-Aminocyclopropanecarboxylic acid
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View Lastest Price from 1-(Boc-amino)cyclopropanecarboxylic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
1-(Boc-amino)cyclopropanecarboxylic acid pictures 2025-09-25 1-(Boc-amino)cyclopropanecarboxylic acid
88950-64-5
US $34.00-1.20 / kg 1kg 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
1-(Boc-amino)cyclopropanecarboxylic acid pictures 2025-04-04 1-(Boc-amino)cyclopropanecarboxylic acid
88950-64-5
US $0.00-0.00 / kg 1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
1-(Boc-amino)cyclopropanecarboxylic acid pictures 2021-08-12 1-(Boc-amino)cyclopropanecarboxylic acid
88950-64-5
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd

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} N-Boc-1-aminocyclopropanecarboxylic acid, CAS 88950-64-5 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