375217
2-氯-4,6-二甲氧基-1,3,5-三嗪
97%
别名:
2,4-二甲氧基-6-氯-1,3,5-三嗪, 2,4-二甲氧基-6-氯-s-三嗪, 2-氯-4,6-二甲氧基-1,3,5-三嗪, 2-氯-4,6-二甲氧基-s-三嗪, 4,6-二甲氧基-2-氯-s-三嗪, 6-氯-2,4-二甲氧基-s-三嗪, CDMT, 氯二甲氧基三嗪
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关于此项目
经验公式（希尔记法）:
C5H6ClN3O2
化学文摘社编号:
分子量:
175.57
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
221-541-0
Beilstein/REAXYS Number:
148988
MDL number:
Assay:
97%
Form:
solid
产品名称
2-氯-4,6-二甲氧基-1,3,5-三嗪, 97%
InChI key
GPIQOFWTZXXOOV-UHFFFAOYSA-N
InChI
1S/C5H6ClN3O2/c1-10-4-7-3(6)8-5(9-4)11-2/h1-2H3
SMILES string
COc1nc(Cl)nc(OC)n1
assay
97%
form
solid
mp
71-74 °C (lit.)
functional group
chloro
Quality Level
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Application
2-氯-4,6-二甲氧基-1,3,5-三嗪可用于以下研究：
- 亲和标记的模块化方法 (MoAL) 对链霉亲和素的特异性标记。
- 通过与 2-羟基-4,6-二甲氧基-1,3,5-三嗪-2-基）醚反应制备双（4,6-二甲氧基-1,3,5-三嗪-2-基）醚。
- 通过与多种叔胺反应制备 2-（4,6-二甲氧基-1,3,5-三嗪基）三烷基铵盐。
- 在四氢呋喃中与 N -甲基吗啉偶联合成 4-（4,6-二甲氧基-1,3,5-三嗪-2-基）-4-甲基吗啉氯化物。
一种稳定并且具高反应性的肽偶联剂。
General description
2-氯-4,6-二甲氧基-1,3,5-三嗪是一种稳定但高度活性的肽偶联剂。它被报道为多肽纯化的有效偶联试剂。已报道 2-氯-4,6-二甲氧基-1,3,5-三嗪的催化酰胺化反应。已报道制备多千克 2-氯-4,6-二甲氧基-1,3,5-三嗪的方法。
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
E Johanna L Stéen et al.
ACS nano, 14(1), 568-584 (2019-12-11)
Tumor targeting using agents with slow pharmacokinetics represents a major challenge in nuclear imaging and targeted radionuclide therapy as they most often result in low imaging contrast and high radiation dose to healthy tissue. To address this challenge, we developed
Synthesis, 917-917 (1987)
Munetaka Kunishima et al.
Chemical & pharmaceutical bulletin, 62(11), 1146-1150 (2014-11-05)
We studied the specific labeling of streptavidin using the modular method for affinity labeling (MoAL) that we developed based on a catalytic amide-forming reaction using 2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT) and a tertiary amine catalyst. The primary structures of avidin and streptavidin are
An improved procedure for the large scale preparation of 2-chloro-4, 6-dimethoxy-1, 3, 5-triazine.
Cronin JS, et al.
Synthetic Communications, 26(!8), 3491-3494 (1996)
2-Chloro-4, 6-dimethoxy-1, 3, 5-triazine. A new coupling reagent for peptide synthesis.
Kaminski ZJ.
Synthesis, 10, 917-920 (1987)
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