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Merck
CN

495018

1-(tert-Butoxycarbonyl)-3-piperidinecarboxylic acid

98%

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About This Item

Empirical Formula (Hill Notation):
C11H19NO4
CAS Number:
Molecular Weight:
229.27
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
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assay

98%

reaction suitability

reaction type: solution phase peptide synthesis

mp

159-162 °C (lit.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N1CCCC(C1)C(O)=O

InChI

1S/C11H19NO4/c1-11(2,3)16-10(15)12-6-4-5-8(7-12)9(13)14/h8H,4-7H2,1-3H3,(H,13,14)

InChI key

NXILIHONWRXHFA-UHFFFAOYSA-N



pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Bunta Watanabe et al.
PloS one, 10(8), e0136242-e0136242 (2015-08-22)
CCG-1423 suppresses several pathological processes including cancer cell migration, tissue fibrosis, and the development of atherosclerotic lesions. These suppressions are caused by inhibition of myocardin-related transcription factor A (MRTF-A), which is a critical factor for epithelial-mesenchymal transition (EMT). CCG-1423 can



Global Trade Item Number

SKUGTIN
495018-5G04061832595016
495018-25G04061832595009