所有图片(1)
About This Item
经验公式（希尔记法）:
C4H9N
CAS号:
分子量:
71.12
FEMA编号:
3523
Beilstein:
102395
EC 号:
欧洲委员会编号:
10491
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
14.064
NACRES:
NA.21
性状检查:
fishy
等级:
Kosher
生物来源:
synthetic
食品过敏原:
no known allergens, no known allergens
推荐产品
生物来源
synthetic
质量水平
等级
Kosher
蒸汽密度
2.45 (vs air)
蒸汽压
128 mmHg ( 39 °C)
49 mmHg ( 20 °C)
方案
≥99%
自燃温度
653 °F
expl. lim.
10.6 %
折射率
n20/D 1.443 (lit.)
密度
0.852 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens, no known allergens
性状检查
fishy
SMILES字符串
C1CCNC1
InChI
1S/C4H9N/c1-2-4-5-3-1/h5H,1-4H2
InChI key
RWRDLPDLKQPQOW-UHFFFAOYSA-N
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其他说明
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警示用语：
Danger
危险分类
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
37.4 °F - closed cup
闪点(°C)
3 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
Y Arun et al.
Bioorganic & medicinal chemistry letters, 23(6), 1839-1845 (2013-02-12)
Novel dispirooxindole-pyrrolidine derivatives have been synthesized through 1,3-dipolar cycloaddition of an azomethine ylide generated from isatin and sarcosine with the dipolarophile 3-(1H-indol-3-yl)-3-oxo-2-(2-oxoindolin-3-ylidene)propanenitrile, and also spiro compound of acenaphthenequinone obtained by the same optimized reaction condition. Synthesized compounds were evaluated for
Hiroaki Chiba et al.
Angewandte Chemie (International ed. in English), 51(36), 9169-9172 (2012-08-15)
In control: The novel and enantioselective total synthesis of (-)-quinocarcin includes the highly stereoselective preparation of the 2,5-cis-pyrrolidine by intramolecular amination, a selective substrate-controlled 6-endo-dig intramolecular alkyne hydroamination with a cationic Au(I) catalyst, and Lewis-acid-mediated ring-opening/halogenation sequence.
Yukari Kondo et al.
The Journal of organic chemistry, 77(18), 7988-7999 (2012-08-18)
We report an enantioselective synthesis of the polyhydroxylated pyrrolidine alkaloid (+)-DMDP. The key steps in the synthesis were guanidinium ylide mediated asymmetric aziridination, stereospecific ring opening of trans-3-vinylaziridine-2-carboxylate with an oxygen nucleophile, iodine-mediated 5-endo-trig amino cyclization, and Prévost displacement. In
Boyu Zhang et al.
Angewandte Chemie (International ed. in English), 51(52), 13159-13162 (2012-11-20)
Drop it! A highly enantioselective catalytic cascade reaction of α-ketoacids and aldehydes is achieved using the title catalyst and water as the solvent. Fluorescence imaging shows that the catalyst is mainly distributed on the surface of emulsion droplets. Optically active
Igor A Kirilyuk et al.
The Journal of organic chemistry, 77(18), 8016-8027 (2012-08-25)
The nitroxides of 7-azadispiro[5.1.5.2]pentadecane and 7-azadispiro[5.1.5.2]pentadeca-14-ene series have been prepared, including thiol-specific methane thiosulfonate spin label for site-directed spin labeling. The effect of spirocyclohexane moieties on chemical and spectral properties has been studied. The obtained temperature dependencies of electron spin
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