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Merck
CN

15033

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
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
57647268
MDL number:
MFCD02683528
Beilstein/REAXYS Number:
7947176

Key Documents

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Product Name

1,3-Di-Boc-2-(trifluoromethylsulfonyl)guanidine, ≥95.0% (HPLC)

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)

SMILES string

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

InChI key

GOQZIPJCBUYLIR-UHFFFAOYSA-N

assay

≥95.0% (HPLC)

form

solid

mp

113 °C (dec.) (lit.)

application(s)

peptide synthesis

Quality Level

100

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Other Notes

Guanidinylation reagents for amines and peptides

pictograms

Exclamation mark
GHS07

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCK1856
BCBQ2141V
BCBG9447V
1434106V
1434106

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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)
Maryam Pourhajibagher et al.
Photodiagnosis and photodynamic therapy, 31, 101834-101834 (2020-05-29)
Antimicrobial photodynamic therapy (aPDT) is a treatment to deal with microorganisms, which is limited to treating microbial biofilms due to poor light penetration. Sonodynamic antimicrobial chemotherapy (SACT) can be used for circumventing the limitations of aPDT to inhibit the polymicrobial

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