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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:
Molecular Weight:
229.27
UNSPSC Code:
12352202
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
478306
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assay

≥98.0% (TLC)

reaction suitability

reaction type: Boc solid-phase peptide synthesis

application(s)

peptide synthesis

SMILES string

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

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

InChI key

GDWKIRLZWQQMIE-QMMMGPOBSA-N

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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Articles

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.


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)



Global Trade Item Number

SKUGTIN
B103268-25ML04061836693480
B103268-5ML04061836693497
14982-1G04061826100592