<生产厂家价格>

间三氟甲基苯乙酮

间三氟甲基苯乙酮用途

用作农药中间体

间三氟甲基苯乙酮名称

[ CAS 号 ]:
349-76-8

[ 中文名 ]:
间三氟甲基苯乙酮

[ 英文名 ]:
3′-(Trifluoromethyl)acetophenone

[中文别名 ]:

[英文别名 ]:

1-Acetyl-3-(trifluoromethyl)benzene
3’-(Trifluoromethyl)acetophenone
Acetophenone, 3'-(trifluoromethyl)-
m-Trifluoromethylacetophenone
1-[3-(Trifluoromethyl)phenyl]ethanone
3′-(Trifluoromethyl)acetophenone
FXFFR CV1
Ethanone, 1-[3-(trifluoromethyl)phenyl]-
EINECS 206-490-4
3'-(TrifluoroMethyl)acetophenone

间三氟甲基苯乙酮物理化学性质

[ 密度 ]:
1.2±0.1 g/cm3

[ 沸点 ]:
199.0±0.0 °C at 760 mmHg

[ 分子式 ]:
C₉H₇F₃O

[ 分子量 ]:
188.146

[ 闪点 ]:
83.9±0.0 °C

[ 精确质量 ]:
188.044907

[ PSA ]:
17.07000

[ LogP ]:
2.72

[ 外观性状 ]:
无色液体

[ 蒸汽压 ]:
0.3±0.3 mmHg at 25°C

[ 折射率 ]:
1.447

[ 储存条件 ]:
室温

间三氟甲基苯乙酮MSDS

详细MSDS(安全技术说明书)

间三氟甲基苯乙酮安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ 危害码 (欧洲) ]:
Xi:Irritant

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
1

[ 海关编码 ]:
29147090

间三氟甲基苯乙酮上下游产品

间三氟甲基苯乙酮上游产品

间三氟甲基苯乙酮下游产品

间三氟甲基苯乙酮海关

[ 海关编码 ]: 2914700090

[ 中文概述 ]:
2914700090 其他酮及醌的卤化、磺化衍生物（包括硝化和亚硝化衍生物）. 增值税率:17.0% 退税率:9.0% 监管条件:无最惠国关税:5.5% 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 丙酮报明包装

[ Summary ]:
HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%

间三氟甲基苯乙酮文献

Highly enantioselective catalytic phenylation of ketones with a constrained geometry titanium catalyst.

Org. Lett. 5(20) , 3641-4, (2003)

[reaction: see text] The catalytic asymmetric addition of phenyl groups from diphenylzinc to ketones is reported. The catalyst, generated from a dihydroxy bis(sulfonamide) ligand and titanium tetraiso...

Asymmetric transfer hydrogenation: chiral ligands and applications.

Chem. Soc. Rev. 35(3) , 226-36, (2006)

Hydrogen transfer reduction processes are attracting increasing interest from synthetic chemists in view of their operational simplicity and high selectivity. In this tutorial review the most signific...

A practical catalytic asymmetric addition of alkyl groups to ketones.

J. Am. Chem. Soc. 124(37) , 10970-1, (2002)

Many catalysts will promote the asymmetric addition of alkylzinc reagents to aldehydes. In contrast, there are no reports of additions to ketones that are both general and highly enantioselective. We ...

更多文献