Merck
CN

A36808

Sigma-Aldrich

N-烯丙基脲

95%

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线性分子式:
CH2=CHCH2NHCONH2
CAS号:
分子量:
100.12
Beilstein:
1745068
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

检测方案

95%

mp

84-86 °C (lit.)

储存温度

2-8°C

SMILES字符串

NC(=O)NCC=C

InChI

1S/C4H8N2O/c1-2-3-6-4(5)7/h2H,1,3H2,(H3,5,6,7)

InChI key

VPJDULFXCAQHRC-UHFFFAOYSA-N

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储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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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
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
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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