66181
N-琥珀酰亚胺基 N-甲基氨基甲酸酯
≥97.0% (N), for peptide synthesis
别名:
MIC 替代品, 异氰酸甲酯替代品
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关于此项目
经验公式（希尔记法）:
C6H8N2O4
化学文摘社编号:
分子量:
172.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Beilstein/REAXYS Number:
1531863
产品名称
N-琥珀酰亚胺基 N-甲基氨基甲酸酯, ≥97.0% (N)
InChI key
XMNGSPOWUCNRMO-UHFFFAOYSA-N
SMILES string
CNC(=O)ON1C(=O)CCC1=O
InChI
1S/C6H8N2O4/c1-7-6(11)12-8-4(9)2-3-5(8)10/h2-3H2,1H3,(H,7,11)
assay
≥97.0% (N)
form
solid
application(s)
peptide synthesis
functional group
amine, imide
storage temp.
2-8°C
Quality Level
Other Notes
有毒的异氰酸甲酯 (MIC) 的安全、结晶状化学等价物。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
K. Takeda et al.
Tetrahedron Letters, 24, 4569-4569 (1983)
J Martinez et al.
Journal of medicinal chemistry, 25(2), 178-182 (1982-02-01)
A practical and convenient method for synthesizing antitumor compounds, N-alkyl-N-nitrosoureas, regioselectively nitrosated on the nitrogen atom bearing the alkyl group is proposed. N-Alkyl-N-nitrosocarbamates are interesting intermediates in these syntheses and yield, by reaction with amino compounds, the regioselectively nitrosated N-alkyl-N-nitrosoureas.
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