A36808
N-烯丙基脲
95%
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线性分子式:
CH2=CHCH2NHCONH2
化学文摘社编号:
分子量:
100.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-157-1
Beilstein/REAXYS Number:
1745068
MDL number:
InChI key
VPJDULFXCAQHRC-UHFFFAOYSA-N
InChI
1S/C4H8N2O/c1-2-3-6-4(5)7/h2H,1,3H2,(H3,5,6,7)
SMILES string
NC(=O)NCC=C
assay
95%
mp
84-86 °C (lit.)
storage temp.
2-8°C
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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
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G R Harper et al.
Biomaterials, 16(6), 427-439 (1995-04-01)
The attachment to rat Kupffer cells of polymeric microspheres, sterically stabilized with different amounts of pendant poly(ethylene oxide) (PEO), was assessed in vitro. Four types of copolymer polystyrene (PS) microspheres were synthesized by variation of four possible monomer ratios that
Jonathan A Fritz et al.
Organic letters, 8(12), 2531-2534 (2006-06-02)
A new strategy for the preparation of substituted imidazolidin-2-ones in two steps from readily available N-allylamines is described. Addition of the amine starting materials to isocyanates affords N-allylureas, which are converted to imidazolidin-2-one products with generation of two bonds and
A Olivier et al.
Biomacromolecules, 1(2), 282-289 (2001-11-17)
A structural and compositional study of thermoplastic blends prepared from native potato starch (NPS) and various amounts of allylurea (AU) was performed to gain a better understanding of possible radiochemical routes to physically stable materials. The blends, mixed at ca.
Naohiko Shimada et al.
Biomacromolecules, 12(10), 3418-3422 (2011-09-21)
There are few examples of polymers that exhibit upper critical solution temperature (UCST) behavior under physiological conditions of temperature, pH, and ionic strength. In this study, we demonstrated that polymers with ureido groups undergo UCST-type phase transitions under physiologically relevant
Daniel J Tetlow et al.
Organic letters, 12(23), 5442-5445 (2010-11-11)
On lithiation with lithium amides, N-allyl-N'-aryl ureas undergo rearrangement with transfer of the aryl ring from N to the allylic α carbon. From the α-arylated products, a further aryl transfer under the influence of a chiral lithium amide allows the
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