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Merck
CN

122882

2-氨基-4-氯-6-甲基嘧啶

97%

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关于此项目

经验公式(希尔记法):
C5H6ClN3
化学文摘社编号:
分子量:
143.57
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
227-018-3
Beilstein/REAXYS Number:
114297
MDL number:
Assay:
97%
Form:
solid
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Quality Level

assay

97%

form

solid

mp

183-186 °C (lit.)

solubility

acetic acid: soluble 50 mg/mL, clear, colorless to faintly yellow

functional group

chloro

SMILES string

Cc1cc(Cl)nc(N)n1

InChI

1S/C5H6ClN3/c1-3-2-4(6)9-5(7)8-3/h2H,1H3,(H2,7,8,9)

InChI key

NPTGVVKPLWFPPX-UHFFFAOYSA-N

General description

2-Amino-4-chloro-6-methylpyrimidine is a nitification inhibitor.

Application

2-Amino-4-chloro-6-methylpyrimidine was used to study the influence of chlorine substitution in pyrimidine ring on proton donor ability of amino group in 2-aminopyrimidine.


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Effects of nitrification inhibitors on denitrification of nitrate in soil.
Bremner JM andYeomans JC.
Biology and Fertility of Soils, 2(4), 173-179 (1986)
T Jayavarthanan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 97, 811-824 (2012-08-21)
The solid phase FTIR and FT-Raman spectra of 2-amino-4-chloro-6-methylpyrimidine (2A4Cl6MP) have been recorded in the regions 400-4000 and 50-4,000 cm(-1), respectively. The spectra have been interpreted interms of fundamentals modes, combination and overtone bands. The structure of the molecule has
Influence of chlorine-substitution in pyrimidine ring on proton donor ability in H-bond and parameters of amino group of 2-amino pyrimidine.
Borisenko VE, et al.
Vibrational Spectroscopy, 37(1), 97-109 (2005)



全球贸易项目编号

货号GTIN
122882-5G04061832241760
122882-25G04061838345554