碳酸二稀丙酯 | 15022-08-9
中文名称:
碳酸二稀丙酯
英文名称:
Diallyl carbonate
CAS No.:
15022-08-9
分子式:
C7 H1 0 O3
分子量:
142.1525
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:碳酸二稀丙酯结构式
名称和标识符
MDL
MFCD00008645
InChIKey
JKJWYKGYGWOAHT-UHFFFAOYSA-N
Inchi
InChI=1S/C7H10O3/c1-3-5-9-7(8)10-6-4-2/h3-4H,1-2,5-6H2
SMILES
C=CCOC(OCC=C)=O
别名信息
- 中文别名 -
碳酸二烯丙酯
碳酸二丙酯烯酯
碳酸二稀丙酯
碳酸丙稀酯
- 英文别名 -
Carbonic acid,di-2-propen-1-yl ester
diallyl carbonate
bis(prop-2-enyl) carbonate
Allyl carbonate
bis-allylcarbonate
Carbonic acid,di-2-propenyl ester
Carbonic acid,diallyl ester
diallyl dicarbonate
ghl.PD_Mitscher_leg0.86
Carbonic acid diallyl
Carbonic acid O,O-diallyl ester
Diallyl carbonate 99%
Carbonic acid, diallyl ester
carbonicacid,di-2-propenylester
Carbonic acid, di-2-propenyl ester
BS-27398
diallylcarbonate
NS00006089
Carbonic acid, di-2-propen-1-yl ester
F87809
EC 239-106-9
DTXSID6065846
NSC19177
NSC-19177
SCHEMBL9928
J9P2G65CXJ
MFCD00008645
15022-08-9
FT-0624599
di-allyl carbonate
Diallyl carbonate
Diallyl carbonate, 99%
EINECS 239-106-9
NSC 19177
AKOS015915885
CS-0204418
DIALLYL CARBONATE
物化性质
实验特性
LogP
1.51160
PSA
35.53000
折射率
n20/D 1.428(lit.)
沸点
95-97 °C60 mm Hg(lit.)
熔点
25°C
闪点
138 °F
颜色与性状
不可用
溶解性
不可用
密度
0.991 g/mL at 25 °C(lit.)
计算特性
精确分子量
142.06300
氢键供体数量
0
氢键受体数量
3
可旋转化学键数量
6
同位素质量
142.062994177g/mol
重原子数量
10
复杂度
115
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)
1.8
互变异构体数量
无
表面电荷
0
拓扑分子极性表面积
35.5Ų
海关数据
海关编码
2920909090
海关数据
中国海关编码:
2920909090
概述:
2920909090 其他无机酸酯(不包括卤化氢的酯)(包括其盐及它们的卤化,磺化,硝化和亚硝化衍生物)。监管条件:无。增值税率:17.0%。退税率:9.0%。最惠国关税:6.5%。普通关税:30.0%
申报要素:
品名, 成分含量, 用途
Summary:
2920909090 esters of other inorganic acids of non-metals (excluding esters of hydrogen halides) and their salts; their halogenated, sulphonated, nitrated or nitrosated derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%
相关文献
1.
Sustainable functionalization of cellulose and starch with diallyl carbonate in ionic liquids
Zafer S?yler,Michael A. R. Meier Green Chem. 2017 19 3899
2.
The reactions of dimethyl carbonate and its derivatives
P. Tundo,M. Musolino,F. Aricò Green Chem. 2018 20 28
3.
Sustainable allylation of organosolv lignin with diallyl carbonate and detailed structural characterization of modified lignin
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4.
Regio- and stereoretentive synthesis of branched, linear (E)- and (Z)-allyl fluorides from allyl carbonates under Ir-catalysis
Elena Benedetto,Matthew Tredwell,Charlotte Hollingworth,Tanatorn Khotavivattana,John M. Brown,Véronique Gouverneur Chem. Sci. 2013 4 89
5.
Pd-Catalyzed three-component decarboxylative coupling reactions between alkylidene pyrazolones, allyl carbonates and active methylene compounds
Heng Zhang,Lu-Yu Cai,Kuo Wang,Hong-Wu Zhao Org. Biomol. Chem. 2022 20 5115
6.
Palladium-catalyzed ortho-vinylation of β-naphthols with α-trifluoromethyl allyl carbonates: one-pot access to naphtho[2,1-b]furans
Chiliveru Priyanka,Muppidi Subbarao,Nagender Punna Org. Biomol. Chem. 2021 19 8241
7.
Formation of allylated quaternary carbon centers via C–O/C–O bond fragmentation of oxalates and allyl carbonates
Haifeng Chen,Yang Ye,Weiqi Tong,Jianhui Fang,Hegui Gong Chem. Commun. 2020 56 454
8.
Stannylated allyl carbonates as versatile building blocks for the diversity oriented synthesis of allylic amines and amides
Christian Bukovec,Uli Kazmaier Org. Biomol. Chem. 2011 9 2743
9.
Rhodium-catalysed direct C–H allylation of N-sulfonyl ketimines with allyl carbonates
Shu-Tao Mei,Nan-Jin Wang,Qin Ouyang,Ye Wei Chem. Commun. 2015 51 2980
10.
Rhodium-catalysed direct C–H allylation of N-sulfonyl ketimines with allyl carbonates
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