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Merck
모든 사진(3)

주요 문서

213535

Sigma-Aldrich

2,4-Dichloro-6-methoxy-1,3,5-triazine

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About This Item

실험식(Hill 표기법):
C4H3Cl2N3O
CAS Number:
Molecular Weight:
179.99
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

bp

132-134 °C/49 mmHg (lit.)

mp

86-88 °C (lit.)

작용기

chloro

SMILES string

COc1nc(Cl)nc(Cl)n1

InChI

1S/C4H3Cl2N3O/c1-10-4-8-2(5)7-3(6)9-4/h1H3

InChI key

JKAPWXKZLYJQJJ-UHFFFAOYSA-N

애플리케이션

2,4-Dichloro-6-methoxy-1,3,5-triazine was used as reagent in radioimmunoassay for D-Ala2-Dermorphin, a natural peptide extracted from amphibian skin. It was also used in the preparation of:




  • α-cyclodextrin [2]-rotaxanes
  • substituted s-triazines
  • series of chiral derivatizing reagents

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

L Negri et al.
Peptides, 2 Suppl 2, 45-49 (1981-01-01)
A selective RIA for D-Ala2-Dermorphin (Der), a natural peptide extracted from amphibian skin, has been developed using an antibody raised in rabbits against Der which has been coupled to BSA through its phenolic hydroxyl groups of tyrosine residues with 2,4-Dichloro-6-methoxy-1,3,5-triazine.
Ryan E Dawson et al.
Organic & biomolecular chemistry, 6(10), 1814-1821 (2008-05-03)
Ten alpha-cyclodextrin [2]-rotaxanes have been prepared with alkane-, stilbene- and azobenzene-based axles, capped through nucleophilic substitution of either 2-chloro-4,6-dimethoxy-1,3,5-triazine or 2,4-dichloro-6-methoxy-1,3,5-triazine in aqueous solution, followed by further substitution of the remaining triazinyl chlorine in some cases when the latter capping
Recent applications of 2, 4, 6-trichloro-1, 3, 5-triazine and its derivatives in organic synthesis.
Blotny G.
Tetrahedron, 62(41), 9507-9522 (2006)
H Brückner et al.
Journal of chromatography. A, 998(1-2), 73-82 (2003-07-17)
A series of chiral derivatizing reagents (CDRs) was synthesized by nucleophilic replacement of one chlorine atom in cyanuric chloride (2,4,6-trichloro-1,3,5-triazine; s-triazine) by alkoxy (methoxy, butoxy, 1,1,1-trifluoroethoxy) or aryloxy groups (phenoxy, nitrophenoxy, phenylphenoxy, 4-methylcoumaryloxy), and displacement of a second chlorine by
Tatsuki Nakano et al.
Analytica chimica acta, 880, 145-151 (2015-06-21)
In this study, a novel pre-column excimer fluorescence derivatization reagent, 2-chloro-4-methoxy-6-(4-(pyren-4-yl)butoxy)-1,3,5-triazine (CMPT), was developed for polyamines, specifically histamine. By CMPT derivatization, the polyamines, histamine and tyramine were converted to polypyrene derivatives, and emitted intra-molecular excimer fluorescence at 475nm. This could

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