178365
1,4-二叠氮-8-壬烯
98%
别名:
4-哌啶酮缩乙二醇
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关于此项目
经验公式（希尔记法）:
C7H13NO2
化学文摘社编号:
分子量:
143.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-868-6
Beilstein/REAXYS Number:
506799
MDL number:
产品名称
1,4-二叠氮-8-壬烯, 98%
InChI key
KPKNTUUIEVXMOH-UHFFFAOYSA-N
InChI
1S/C7H13NO2/c1-3-8-4-2-7(1)9-5-6-10-7/h8H,1-6H2
SMILES string
C1CC2(CCN1)OCCO2
assay
98%
form
liquid
refractive index
n20/D 1.4819 (lit.)
bp
108-111 °C/26 mmHg (lit.)
density
1.117 g/mL at 20 °C (lit.)
functional group
ether
ketal
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Application
1,4-Dioxa-8-azaspiro[4.5]decane was used in the synthesis of 1,4-dioxa-8-azaspiro [4,5] deca spirocyclotriphosphazenes.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
177.8 °F - closed cup
flash_point_c
81 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Nuran Asmafiliz et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 86, 214-223 (2011-11-23)
The Schiff base compounds (1 and 2) are synthesized by the condensation reactions of 2-furan-2-yl-methylamine with 2-hydroxy-3-methoxy- and 2-hydroxy-5-methoxy-benzaldehydes and reduced with NaBH(4) to give the new N/O-donor-type ligands (3 and 4). The monospirocyclotriphosphazenes containing 1,3,2-oxazaphosphorine rings (5 and 6)
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