1,3-二苄基脲 | 1466-67-7
中文名称:
1,3-二苄基脲
英文名称:
1,3-Dibenzylurea
CAS No.:
1466-67-7
分子式:
C1 5 H1 6 N2 O
分子量:
240.30034
名称和标识符
MDL
MFCD00276302
InChIKey
KATOLVAXCGIBLO-UHFFFAOYSA-N
Inchi
InChI=1S/C15H16N2O/c18-15(16-11-13-7-3-1-4-8-13)17-12-14-9-5-2-6-10-14/h1-10H,11-12H2,(H2,16,17,18)
SMILES
O=C(NCC1=CC=CC=C1)NCC2=CC=CC=C2
别名信息
- 英文别名 -
Urea,N,N'-bis(phenylmethyl)-
1,3-DIBENZYL UREA
N,N'-Dibenzylharnstoff
N,N'-Dibenzylurea
sym-Dibenzylurea
1,3-bis(benzyl)urea
1,3-bis(phenylmethyl)urea
doi:10.14272/KATOLVAXCGIBLO-UHFFFAOYSA-N.1
BDBM50248768
1,3-Dibenzyl-urea
AB89805
AMY18868
1,3-dibenzyl urea
MFCD00276302
SCHEMBL714625
A909424
NSC 408007
AI3-19855
dibenzylurea
BAA46667
Z56896289
ZV725XJ34V
AKOS000312988
PD179184
CHEMBL504463
DTXSID3061710
SR-01000638399-1
Urea, N,N'-bis(phenylmethyl)-
EINECS 215-984-9
N,N'-BIS(PHENYLMETHYL)UREA
CCG-48904
W13186
FS-5664
1,3-Dibenzylurea
NSC408007
10.14272/KATOLVAXCGIBLO-UHFFFAOYSA-N.1
HMS1697A06
Oprea1_448978
NS00024797
InChI=1/C15H16N2O/c18-15(16-11-13-7-3-1-4-8-13)17-12-14-9-5-2-6-10-14/h1-10H,11-12H2,(H2,16,17,18
EN300-04024
Urea,N'-bis(phenylmethyl)-
1466-67-7
NSC-408007
CS-0149842
UNII-ZV725XJ34V
1,3-dibenzylurea
物化性质
实验特性
计算特性
精确分子量
240.12638
氢键供体数量
2
氢键受体数量
3
可旋转化学键数量
6
同位素质量
240.126263138g/mol
重原子数量
18
复杂度
219
同位素原子数量
0
确定原子立构中心数量
0
不确定原子立构中心数量
0
确定化学键立构中心数量
0
不确定化学键立构中心数量
0
共价键单元数量
1
疏水参数计算参考值(XlogP)
2.4
拓扑分子极性表面积
41.1Ų
相关文献
1.
Direct extraction of carbonyl from waste polycarbonate with amines under environmentally friendly conditions: scope of waste polycarbonate as a carbonylating agent in organic synthesis
Sukhdeep Singh,Yong Lei,Andreas Schober RSC Adv. 2015 5 3454
2.
Enantioselective synthesis of hydantoins by chiral acid-catalysed condensation of glyoxals and ureas
Sushant Aryal,Christopher A. Hone,Matthew I. J. Polson,Daniel J. Foley Chem. Sci. 2023 14 7905
3.
To gel or not to gel: correlating molecular gelation with solvent parameters
Y. Lan,M. G. Corradini,R. G. Weiss,S. R. Raghavan,M. A. Rogers Chem. Soc. Rev. 2015 44 6035
4.
Amine synthesis via transition metal homogeneous catalysed hydrosilylation
Bin Li,Jean-Baptiste Sortais,Christophe Darcel RSC Adv. 2016 6 57603
5.
Recent advances in multi-component reactions and their mechanistic insights: a triennium review
Stephy Elza John,Shivani Gulati,Nagula Shankaraiah Org. Chem. Front. 2021 8 4237
6.
Ureas as safe carbonyl sources for the synthesis of carbamates with deep eutectic solvents (DESs) as efficient and recyclable solvent/catalyst systems
Iman Dindarloo Inaloo,Sahar Majnooni New J. Chem. 2018 42 13249
7.
Full atom-efficiency transformation of wasted polycarbonates into epoxy thermosets and the catalyst-free degradation of the thermosets for environmental sustainability
Shih Wei Shao,Chien Han Chen,Jian Ren Chan,Tzong Yuan Juang,Mahdi M. Abu-Omar,Ching Hsuan Lin Green Chem. 2020 22 4683
8.
Structure and activity relationship studies of N-heterocyclic olefin and thiourea/urea catalytic systems: application in ring-opening polymerization of lactones
Li Zhou,Zhenyu Wang,Guangqiang Xu,Chengdong Lv,Qinggang Wang Polym. Chem. 2021 12 1806
9.
A practical stereospecific synthesis of the biotin precursor (3aα,6aα)-1,3-dibenzylhexahydro-1H-thieno[3,4-d]imidazol-2(3H)-one 1,1-dioxide
Hans Aaron Bates,Lloyd Smilowitz,Stuart B. Rosenblum J. Chem. Soc. Chem. Commun. 1985 353
10.
A practical stereospecific synthesis of the biotin precursor (3aα,6aα)-1,3-dibenzylhexahydro-1H-thieno[3,4-d]imidazol-2(3H)-one 1,1-dioxide
Hans Aaron Bates,Lloyd Smilowitz,Stuart B. Rosenblum J. Chem. Soc. Chem. Commun. 1985 353
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