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15033

Sigma-Aldrich

1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine

≥95.0% (HPLC)

Synonym(s):

N,N′-Bis(tert-butoxycarboyl)-N′′-trifylguanidine

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About This Item

Linear Formula:
CF3SO2N=C[NHCO2C(CH3)3]2
CAS Number:
207857-15-6
Molecular Weight:
391.36
Beilstein:
7947176
MDL number:
MFCD02683528
UNSPSC Code:
12352200
PubChem Substance ID:
57647268
NACRES:
NA.22

Quality Level

100

Assay

≥95.0% (HPLC)

form

solid

mp

113 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N\C(NC(=O)OC(C)(C)C)=N\S(=O)(=O)C(F)(F)F

InChI

1S/C12H20F3N3O6S/c1-10(2,3)23-8(19)16-7(17-9(20)24-11(4,5)6)18-25(21,22)12(13,14)15/h1-6H3,(H2,16,17,18,19,20)

InChI key

GOQZIPJCBUYLIR-UHFFFAOYSA-N

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Related Categories

Other Notes

Guanidinylation reagents for amines and peptides

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - 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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Abdelkader A Metwally et al.
Pharmaceutics, 3(3), 406-424 (2011-01-01)
Four guanidine derivatives of N4,N9-diacylated spermine have been designed, synthesized, and characterized. These guanidine-containing cationic lipids bound siRNA and formed nanoparticles. Two cationic lipids with C18 unsaturated chains, N1,N12-diamidino-N4,N9-dioleoylspermine and N1,N12-diamidino-N4-linoleoyl-N9-oleoylspermine, were more efficient in terms of GFP expression reduction
Tom S Carter et al.
Angewandte Chemie (International ed. in English), 55(32), 9311-9315 (2016-06-18)
Biomimetic carbohydrate receptors ("synthetic lectins") have potential as agents for biological research and medicine. However, although effective strategies are available for "all-equatorial" carbohydrates (glucose, etc.), the recognition of other types of saccharide under natural (aqueous) conditions is less well developed.
K. Feichtinger et al.
The Journal of Organic Chemistry, 63, 8432-8432 (1998)

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