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Merck
모든 사진(1)

주요 문서

391387

Sigma-Aldrich

4-Amino-5-chloro-2,6-dimethylpyrimidine

96%

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About This Item

실험식(Hill 표기법):
C6H8ClN3
CAS Number:
Molecular Weight:
157.60
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

96%

mp

164-166 °C (lit.)

SMILES string

Cc1nc(C)c(Cl)c(N)n1

InChI

1S/C6H8ClN3/c1-3-5(7)6(8)10-4(2)9-3/h1-2H3,(H2,8,9,10)

InChI key

BKFCZKYCVQQMCX-UHFFFAOYSA-N

일반 설명

4-Amino-5-chloro-2,6-dimethylpyrimidine (ACDP) is an aminopyrimidine derivative. Its interaction as an electron donor with a σ-electron acceptor, iodine has been studied.
4-Amino-5-chloro-2,6-dimethylpyrimidine participates in the synthesis of diazino[c]quinolin-5(6H)-one and -isoquinolin-6(5H)-one, diazino[c]naphthyridin-6(5H)- and -5(6H)-one derivatives.

애플리케이션

4-Amino-5-chloro-2,6-dimethylpyrimidine is suitable reagent employed as a nucleobase standard in the systematic quantitative structure-retention relationship (QSRR) study on pyrimidines between the molecular descriptors (variables) and their chromatographic retention (experimental unit).

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)

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문서 라이브러리 방문

Synthesis of substituted diazino[c] quinolin-5(6H)-ones, diazino[c]isoquinolin-6(5H)-ones, diazino [c]naphthyridin-6(5H)-ones and diazino[c]naphthyridin-5(6H)-ones.
Fresneau N, et al.
Tetrahedron, 69(26), 5393-5400 (2013)
Usama M Rabie et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(3), 605-611 (2007-02-24)
Interactions of some pyrimidine derivatives, 4-amino-2,6-dimethylpyrimidine, kyanmethin, (4AP), 2-amino-4,6-dimethylpyrimidine (2AP), 2-aminopyrimidine (AP), 2-amino-4-methylpyrimidine (AMP), 2-amino-4-methoxy-6-methylpyrimidine (AMMP), and 4-amino-5-chloro-2,6-dimethylpyrimidine (ACDP) as electron donors, with iodine (I(2)), as a typical sigma-electron acceptor, have been studied. Electronic absorption spectra of these interactions in
Multivariate Chemometric Study on the Interfacial Properties of Nucleic-Acid Bases.
Luo HB, et al.
Journal of Data Science, 1(4), 447-460 (2003)

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