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Boc-L-beta-Homoproline

CAS No.
56502-01-3
Chemical Name:
Boc-L-beta-Homoproline
Synonyms
Boc-b-HoPro-OH;Boc-β-HoPro-OH;BOC-BETA-HPRO-OH;Boc-β-HomoPro-OH;Boc-p-HomoPro-OH;BOC-BETA-HOPRO-OH;BOC-BETA3-HOMOPRO;BOC-PRO-(C*CH2)OH;boc-β3-homopro-oh;BOC-B-HOMOPROLINE
CBNumber:
CB5169171
Molecular Formula:
C11H19NO4
Molecular Weight:
229.27
MDL Number:
MFCD01862939
MOL File:
56502-01-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:59:00
Product description Number Pack Size Price
Boc-β3-Homopro-OH ≥98.0% (TLC) 14982 1g $85
BOC-L-BETA-HOMOPROLINE 97% 56180 1G $82
BOC-L-BETA-HOMOPROLINE 97% 56180 5G $250
BOC-L-BETA-HOMOPROLINE 97% 56180 10G $480
(S)-2-(1-Boc-2-pyrrolidinyl)acetic Acid 95% B8970 100mg $22
More product size

Boc-L-beta-Homoproline Properties

Melting point 98 °C
Boiling point 357.4±15.0 °C(Predicted)
Density 1.151±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka 4.56±0.10(Predicted)
form Crystalline Powder
color White to off-white
BRN 478306
Major Application peptide synthesis
InChI InChI=1S/C11H19NO4/c1-11(2,3)16-10(15)12-6-4-5-8(12)7-9(13)14/h8H,4-7H2,1-3H3,(H,13,14)/t8-/m0/s1
InChIKey GDWKIRLZWQQMIE-QMMMGPOBSA-N
SMILES N1(C(OC(C)(C)C)=O)CCC[C@H]1CC(O)=O
CAS DataBase Reference 56502-01-3(CAS DataBase Reference)
UNSPSC Code 12352202
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H335-H319-H315
Precautionary statements  P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
PPE Eyeshields, Gloves, type N95 (US)
Safety Statements  24/25
WGK Germany  3
HazardClass  IRRITANT
HS Code  29339900
Storage Class 11 - Combustible Solids
NFPA 704
1
2 0

Boc-L-beta-Homoproline price More Price(60)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 14982 Boc-β3-Homopro-OH ≥98.0% (TLC) 56502-01-3 1g $85 2023-06-20 Buy
AstaTech 56180 BOC-L-BETA-HOMOPROLINE 97% 56502-01-3 1G $82 2026-04-30 Buy
AstaTech 56180 BOC-L-BETA-HOMOPROLINE 97% 56502-01-3 5G $250 2026-04-30 Buy
AstaTech 56180 BOC-L-BETA-HOMOPROLINE 97% 56502-01-3 10G $480 2026-04-30 Buy
Synthonix B8970 (S)-2-(1-Boc-2-pyrrolidinyl)acetic Acid 95% 56502-01-3 100mg $22 2026-05-06 Buy
Product number Packaging Price Buy
14982 1g $85 Buy
56180 1G $82 Buy
56180 5G $250 Buy
56180 10G $480 Buy
B8970 100mg $22 Buy

Boc-L-beta-Homoproline Chemical Properties,Uses,Production

Uses

Building block for necine alkaloids.

Uses

Boc-L-beta-homoproline is an amino acid derivative which is a reagent in the synthesis of dihydroisoxazole inhbitors of human transglutaminase 2, an enzyme that catalyzes the modification of glutamine residues. This enzyme has been implicated in numerous inflmmatory, fibrotic and other diseases.

reaction suitability

reaction type: Boc solid-phase peptide synthesis

Synthesis

METHYL (2S)-PYRROLIDIN-2-YLACETATE

88790-37-8

Boc-L-beta-Homoproline

56502-01-3

General procedure for the synthesis of (S)-2-(2-pyrrolidinyl)acetic acid from methyl (S)-2-(2-pyrrolidinyl)acetate: tert-butyl (2S)-2-(2-methoxy-2-oxoethyl)-1-pyrrolidinecarboxylate (8.35 g, 34.3 mmol) was dissolved in 150 mL of methanol. 50 mL of 1 M aqueous sodium hydroxide solution was added and the reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the solution was concentrated under reduced pressure to about 100 mL. The concentrated solution was added to 300 mL of water and extracted twice with ether (2 x 100 mL). The aqueous phase was acidified to pH 2 with 12N hydrochloric acid and extracted with ether twice more (2 x 100 mL). The aqueous layer was saturated with saturated sodium chloride solution and then extracted with ether a third time (100 mL). All organic layers were combined, washed sequentially with water and saturated sodium chloride solution, and then dried with anhydrous magnesium sulfate. The desiccant was removed by filtration and the filtrate was concentrated under reduced pressure to afford the title compound (S)-2-(1-tert-butoxycarbonyl-2-pyrrolidinyl)acetic acid as a white solid (7.28 g, 31.7 mmol, 92.6% yield). peaks, 4H), 1.48 (single peak, 9H) ppm.

References

[1] Patent: WO2003/76440, 2003, A1. Location in patent: Page/Page column 140
[2] Journal of Organic Chemistry, 2005, vol. 70, # 22, p. 8730 - 8733
[3] Organic and Biomolecular Chemistry, 2003, vol. 1, # 22, p. 3977 - 3988
[4] Tetrahedron Letters, 1997, vol. 38, # 20, p. 3609 - 3610

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View Lastest Price from Boc-L-beta-Homoproline manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Boc-L-beta-Homoproline pictures 2025-04-04 Boc-L-beta-Homoproline
56502-01-3
US $0.00-0.00 / kg 1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
Boc-L-beta-Homoproline pictures 2019-07-06 Boc-L-beta-Homoproline
56502-01-3
US $1.00 / kg 1kg 98% 100KG Career Henan Chemical Co

Boc-L-beta-Homoproline Spectrum

N-BOC-(2S)-PYRR(2-CHCOOH) N-BETA-T-BUTOXYCARBONYL-L-BETA-HOMOPROLINE (S)-2-(1-BOC-2-PYRROLIDINYL)ACETIC ACID (S)-N-T-BUTOXYCARBONYL-PYRROLIDINE-2-ACETIC ACID BOC-L-BETA-HOMOPROLINE BOC-BETA3-HOMOPRO BOC-BETA-HOPRO-OH BOC-BETA-HOMOPROLINE BOC-BETA-HOMOPRO-OH BOC-PRO-(C*CH2)OH Boc-L-beta(3)-homoproline Boc-L-b-homoproline boc-β3-homopro-oh BOC-B-HOMOPROLINE Boc-L-β-Homo-Pro-OH Boc-L-beta-HPro-OH N-beta-(t-Butyloxycarbonyl)-L-homoproline, (S)-N-t-Butyloxycarbonyl-2-(pyrrolidin-2-yl)acetic acid Boc-b-HoPro-OH 2-[(2S)-(1-tert-Butoxycarbonyl)pyrrolidin-2-yl]acetic acid (S)-2-(1-Boc-2-pyrrolidinyl)acetic acid, Boc-L-β3-homoproline Boc-beta-HoPro-OH 56502- Boc-L-β-homoproline≥ 98% (NMR) 2-[(2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidin-2-yl]acetic acid BOC-BETA-HPRO-OH (S)-2-(carboxymethyl)pyrrolidinium chloride Boc-L-beta-homo-Pro (S)-2-Carboxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester Boc-L-β-homoproline ,98% (S)-2-(1-(tert-Butoxycarbonyl)pyrrolidin-2-yl)acetic acid 2-Pyrrolidineacetic acid, 1-[(1,1-diMethylethoxy)carbonyl]-, (2S)- (S)-N-t-Butyloxycarbonyl-2-(pyrrolidin-2-yl)acetic acid N-beta-(t-Butyloxycarbonyl)-L-homoproline Boc-β-HomoPro-OH Boc-beta3-Homopro-OH Boc-L-β-Homoproline Boc-p-HomoPro-OH Boc-L-beta-Homoproline USP/EP/BP Boc-β-HoPro-OH (2S)-1-tert-butoxycarbonyl-2-carboxymethylpyrrolidine Boc-β3-Homopro-OH (S)-2-(1-Bocpyrrolidin-2-yl)-acetic acid 56502-01-3 C11H19N1O4 Specialty Synthesis Peptide Synthesis Unnatural Amino Acid Derivatives Beta-Amino Acids β-Homo Amino Acids Beta amino acids