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经验公式(希尔记法):
C5H2Cl2N4
化学文摘社编号:
分子量:
189.00
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-681-6
Beilstein/REAXYS Number:
9354
MDL number:
产品名称
2,6-二氯嘌呤, 97%
InChI key
RMFWVOLULURGJI-UHFFFAOYSA-N
InChI
1S/C5H2Cl2N4/c6-3-2-4(9-1-8-2)11-5(7)10-3/h1H,(H,8,9,10,11)
SMILES string
Clc1nc(Cl)c2nc[nH]c2n1
assay
97%
form
powder
mp
185-195 °C (dec.) (lit.)
Quality Level
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Application
用于水-乙腈中卤化嘌呤和芳基硼酸的 Suzuki-Miyaura 交叉偶联反应。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Synthesis, 3515-3515 (2006)
M Eugenia García-Rubiño et al.
Acta crystallographica. Section C, Crystal structure communications, 67(Pt 12), o484-o486 (2011-12-06)
Two polymorphs of 2,6-dichloropurine, C(5)H(2)Cl(2)N(4), have been crystallized and identified as the 9H- and 7H-tautomers. Despite differences in the space group and number of symmetry-independent molecules, they exhibit similar hydrogen-bonding motifs. Both crystal structures are stabilized by intermolecular N-H···N interactions
Occupational contact sensitization to 2,6-dichloropurine.
R J Rycroft
Contact dermatitis, 7(3), 162-163 (1981-05-01)
T Maruyama et al.
Nucleosides, nucleotides & nucleic acids, 19(7), 1193-1203 (2000-09-22)
A general procedure to obtain tetra-substituted uric acid by stepwise N-alkylation is described. 2,6-Dichloropurine (1) was condensed with 1-propanol by Mitsunobu reaction to give 9-propyl congener (2). Treatment of 2 with ammonia gave adenine derivative (4a), which was converted to
Occupational contact sensitization to 2,6-dichloropurine.
R J Rycroft
Contact dermatitis, 7(6), 349-350 (1981-11-01)
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