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线性分子式:
(CH3CH2CH2CH2)4N(CN)
化学文摘社编号:
分子量:
268.48
EC Number:
233-926-0
UNSPSC Code:
12352116
PubChem Substance ID:
Beilstein/REAXYS Number:
3598808
MDL number:
InChI key
KRRBFUJMQBDDPR-UHFFFAOYSA-N
InChI
1S/C16H36N.CN/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;1-2/h5-16H2,1-4H3;/q+1;-1
SMILES string
[C-]#N.CCCC[N+](CCCC)(CCCC)CCCC
grade
purum
assay
≥95.0% (AT)
form
crystalline
mp
89-92 °C (lit.)
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Other Notes
合成腈的试剂;制备与氰化亚铜形成的络合物,以及用作偶联剂;转酯化反应的温和试剂
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1
supp_hazards
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
H. Kobler et al.
Justus Liebigs Annalen der Chemie, 1946-1946 (1978)
J.I. Luengo et al.
Tetrahedron Letters, 34, 4599-4599 (1993)
E.J. Corey et al.
Tetrahedron Letters, 25, 5115-5115 (1984)
O.D. Dailey et al.
The Journal of Organic Chemistry, 45, 216-216 (1980)
Fabio Galeotti et al.
Journal of chromatography. A, 1284, 141-147 (2013-03-05)
In this study, by using tetrabutylammonium bisulfate as ion-pairing reagent, we were able to separate all the main heparin/heparan sulfate disaccharides generated by the action of heparinases along with the main Hep tetrasaccharide possessing a 3-O-sulfate group on the sulfoglucosamine
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