跳转至内容
Merck
CN

A52153

Sigma-Aldrich

1,3-二甲基-6-氨基脲嘧啶

98%

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C6H9N3O2
CAS号:
分子量:
155.15
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

98%

表单

powder

mp

295 °C (dec.) (lit.)

SMILES字符串

CN1C(N)=CC(=O)N(C)C1=O

InChI

1S/C6H9N3O2/c1-8-4(7)3-5(10)9(2)6(8)11/h3H,7H2,1-2H3

InChI key

VFGRNTYELNYSKJ-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Wafaa S Hamama et al.
Journal of advanced research, 4(2), 115-121 (2013-03-01)
The reaction of 6-amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione (1) as a binucleophile with primary aromatic or heterocyclic amines and formaldehyde or aromatic (heterocyclic) aldehydes in a molar ratio (1:1:2) gave the pyrimido[4,5-d]pyrimidin-2,4-dione ring systems 2-5. Treatment of 1 with diamines and formalin in molar
Javier Campanini-Salinas et al.
Molecules (Basel, Switzerland), 23(7) (2018-07-22)
A rapid emergence of resistant bacteria is occurring worldwide, endangering the efficacy of antibiotics and reducing the therapeutic arsenal available for treatment of infectious diseases. In the present study, we developed a new class of compounds with antibacterial activity obtained

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门