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Safety Information

03582

Sigma-Aldrich

1-(Boc-amino)cyclohexanecarboxylic acid

≥98.0% (TLC)

Synonym(s):

Boc-homocycloleucine

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About This Item

Linear Formula:
(CH3)3CO2CNHC6H10CO2H
CAS Number:
115951-16-1
Molecular Weight:
243.30
Beilstein:
4189683
MDL number:
MFCD00273427
UNSPSC Code:
12352200
PubChem Substance ID:
329747735
NACRES:
NA.22

Quality Level

100

Assay

≥98.0% (TLC)

form

powder with small lumps

reaction suitability

reaction type: Boc solid-phase peptide synthesis

color

white

mp

176-178 °C (dec.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)NC1(CCCCC1)C(O)=O

InChI

1S/C12H21NO4/c1-11(2,3)17-10(16)13-12(9(14)15)7-5-4-6-8-12/h4-8H2,1-3H3,(H,13,16)(H,14,15)

InChI key

URBHKVWOYIMKNO-UHFFFAOYSA-N

Other Notes

Synthesis of modified peptides

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

03582-1G:
03582-BULK:
03582-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
1431360V
1431360
1342336
436982/1
426614/1

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P Furet et al.
Bioorganic & medicinal chemistry letters, 10(20), 2337-2341 (2000-10-31)
Based on X-ray crystal structure information, mono charged phosphinate isosteres of phosphotyrosine have been designed and incorporated in a short inhibitory peptide sequence of the Grb2-SH2 domain. The resulting compounds, by exploiting additional interactions, inhibit binding to the Grb2-SH2 domain
M Mazzeo et al.
Journal of peptide science : an official publication of the European Peptide Society, 1(5), 330-340 (1995-09-01)
The cyclic octapeptide cyclo[-Pro1-Pro-Phe-Phe-Ac6c-Ile-ala-Val8-] [C8-Ac6c], containing the Pro1-Pro-Phe-Phe sequence, followed by a bulky helicogenic C alpha,alpha-dialkylated glycine residue Ac6c [1-aminocyclohexane-1-carboxylic acid), and a D-Ala residue at position 7 has been synthesized. This cyclic peptide is a deletion analogue of the

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