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06594

(S)-α-Allyl-proline hydrochloride

Name: <I>(S)</I>-α-Allyl-proline hydrochloride
Brand: SIAL

purum, ≥98.0% (TLC)

Synonym(s):

α-Allyl-D-proline hydrochloride, (S)-2-Allyl-2-pyrrolidinecarboxylic acid hydrochloride

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About This Item

Empirical Formula (Hill Notation):

C₈H₁₃NO₂· HCl

CAS Number:

129704-91-2

Molecular Weight:

191.66

NACRES:

NA.22

PubChem Substance ID:

329748251

UNSPSC Code:

12352200

MDL number:

MFCD06659238

Assay:

≥98.0% (TLC)

Form:

powder or crystals

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Properties

Quality Segment

100

grade

purum

assay

≥98.0% (TLC)

form

powder or crystals

reaction suitability

reaction type: solution phase peptide synthesis

color

off-white to brown

mp

186-190 °C

application(s)

peptide synthesis

SMILES string

Cl.OC(=O)[C@]1(CCCN1)CC=C

InChI

1S/C8H13NO2.ClH/c1-2-4-8(7(10)11)5-3-6-9-8;/h2,9H,1,3-6H2,(H,10,11);1H/t8-;/m1./s1

InChI key

DIYYEOOBZVTROL-DDWIOCJRSA-N

Description

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 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.

Emily M Christensen et al.

The Journal of biological chemistry, 295(52), 18316-18327 (2020-10-29)

Pyrroline-5-carboxylate reductase 1 (PYCR1) catalyzes the biosynthetic half-reaction of the proline cycle by reducing Δ1-pyrroline-5-carboxylate (P5C) to proline through the oxidation of NAD(P)H. Many cancers alter their proline metabolism by up-regulating the proline cycle and proline biosynthesis, and knockdowns of

Global Trade Item Number

SKU	GTIN
06594-500MG-F	04061832593081