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Home Other Building Blocks 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride

CAS No.:
3945-69-5
Catalog Number:
AG00363E
Molecular Formula:
C10H17ClN4O3
Molecular Weight:
276.7200
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$13
- +
25g
95%
In Stock USA
United States
$32
- +
100g
95%
In Stock USA
United States
$100
- +
500g
95%
In Stock USA
United States
$450
- +
Product Description
Catalog Number:
AG00363E
Chemical Name:
4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride
CAS Number:
3945-69-5
Molecular Formula:
C10H17ClN4O3
Molecular Weight:
276.7200
MDL Number:
MFCD03613550
IUPAC Name:
4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium;chloride
InChI:
InChI=1S/C10H17N4O3.ClH/c1-14(4-6-17-7-5-14)8-11-9(15-2)13-10(12-8)16-3;/h4-7H2,1-3H3;1H/q+1;/p-1
InChI Key:
BMTZEAOGFDXDAD-UHFFFAOYSA-M
SMILES:
COc1nc(nc(n1)OC)[N+]1(C)CCOCC1.[Cl-]
EC Number:
447-230-1
Properties
Complexity:
236  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
276.099g/mol
Formal Charge:
0
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
276.721g/mol
Monoisotopic Mass:
276.099g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
66.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
Title Journal
Aqueous microwave-assisted solid-phase peptide synthesis using Fmoc strategy. III: racemization studies and water-based synthesis of histidine-containing peptides. Amino acids 20141001
Selective monobenzoylation of 1,2- and 1,3-diols catalyzed by Me2SnCl2 in water (organic solvent free) under mild conditions. The Journal of organic chemistry 20120106
One-pot preparation of Oxazol-5(4H)-ones from amino acids in aqueous solvents. Chemical & pharmaceutical bulletin 20120101
Fluorous derivatization and fluorous-phase separation for fluorometric determination of naproxen and felbinac in human plasma. Journal of pharmaceutical and biomedical analysis 20110428
An in-depth analysis of polymer-analogous conjugation using DMTMM. Bioconjugate chemistry 20110316
An approach towards efficient peptide synthesis in aqueous solution. Acta poloniae pharmaceutica 20100101
Novel acyclic amide-conjugated nucleosides and their analogues. Nucleosides, nucleotides & nucleic acids 20090201
[Studies on reaction control and development of new practical reagents based on characteristics of reaction field]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20080301
DMT-MM mediated functionalisation of the non-reducing end of glycosaminoglycans. Chemical communications (Cambridge, England) 20070714
A novel chemistry for conjugating pneumococcal polysaccharides to Luminex microspheres. Journal of immunological methods 20060220
Solid phase peptide synthesis in water VI: evaluation of water-soluble coupling reagents for solid phase peptide synthesis in aqueous media. Protein and peptide letters 20060101
N-triazinylammonium tetrafluoroborates. A new generation of efficient coupling reagents useful for peptide synthesis. Journal of the American Chemical Society 20051207
Development of a simple system for dehydrocondensation using solid-phase adsorption of a water-soluble dehydrocondensing reagent (DMT-MM). Chemical & pharmaceutical bulletin 20041001
Preparation of Weinreb amides using 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM). Chemical & pharmaceutical bulletin 20040401
A racemization test in peptide synthesis using 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM). Chemical & pharmaceutical bulletin 20020401
Properties