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Merck
CN

14982

Boc-β3-Homopro-OH

≥98.0% (TLC)

Synonym(s):

(S)-2-(1-Boc-2-pyrrolidinyl)acetic acid, Boc-L-β3-homoproline

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About This Item

Empirical Formula (Hill Notation):
C11H19NO4
CAS Number:
56502-01-3
Molecular Weight:
229.27
UNSPSC Code:
12352202
NACRES:
NA.22
PubChem Substance ID:
57647241
MDL number:
MFCD01862939
Beilstein/REAXYS Number:
478306

Key Documents

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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

SMILES string

CC(C)(C)OC(=O)N1CCC[C@H]1CC(O)=O

InChI key

GDWKIRLZWQQMIE-QMMMGPOBSA-N

assay

≥98.0% (TLC)

reaction suitability

reaction type: Boc solid-phase peptide synthesis

application(s)

peptide synthesis

Other Notes

Building block for necine alkaloids; Synthesis of new analogs of arginine-vasopressin.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCBJ5251V
BCBD4681V
BCBB6159V
BCBB6159
1425370

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D.W. Knight et al.
Journal of the Chemical Society. Perkin Transactions 1, 1615-1615 (1991)
K. Bankowski et al.
Collection of Czechoslovak Chemical Communications, 54, 2795-2795 (1989)

Articles

Proline Derivatives and Analogs

Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.

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