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4-(三氟甲基)苄醇

4-(三氟甲基)苄醇用途

【用途一】
用作医药中间体

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4-(三氟甲基)苄醇名称

[ CAS 号 ]:
349-95-1

[ 中文名 ]:
4-(三氟甲基)苄醇

[ 英文名 ]:
(4-(Trifluoromethyl)phenyl)methanol

[中文别名 ]:

[英文别名 ]:

Q1R DXFFF
[4-(Trifluoromethyl)phenyl]methanol
4-(Trifluoromethyl)benzylic alcohol
(4-(Trifluoromethyl)phenyl)methanol
EINECS 206-494-6
3-(trifluoromethyl)benzyl alcohol
4-(Trifluoromethyl)benzyl alcohol
4-trifluoromethylbenzyl alcohol
MFCD00004661
4-(Hydroxymethyl)benzotrifluoride

4-(三氟甲基)苄醇物理化学性质

[ 密度 ]:
1.3±0.1 g/cm3

[ 沸点 ]:
213.7±0.0 °C at 760 mmHg

[ 熔点 ]:
22-25 °C

[ 分子式 ]:
C₈H₇F₃O

[ 分子量 ]:
176.136

[ 闪点 ]:
100.6±0.0 °C

[ 精确质量 ]:
176.044907

[ PSA ]:
20.23000

[ LogP ]:
1.61

[ 外观性状 ]:
白色固体

[ 蒸汽压 ]:
0.1±0.4 mmHg at 25°C

[ 折射率 ]:
1.463

[ 储存条件 ]:
室温

4-(三氟甲基)苄醇MSDS

4-(三氟甲基)苄醇安全信息

[ 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-S37/39

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

[ WGK德国 ]:
3

[ 海关编码 ]:
29062900

4-(三氟甲基)苄醇合成路线

4-(三氟甲基)苄醇上下游产品

4-(三氟甲基)苄醇上游产品

4-(三氟甲基)苄醇下游产品

4-(三氟甲基)苄醇海关

[ 海关编码 ]: 2906299090

[ 中文概述 ]:
2906299090 其他芳香醇. 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

[ Summary ]:
2906299090 other aromatic alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

4-(三氟甲基)苄醇文献

Determination of the equilibrium distibution between alcohol and aldehyde substrates when bound to horse liver alcohol dehydrogenase using magnetic resonance.

Biochemistry 19(24) , 5486-93, (1980)

The interactions of horse liver alcohol dehydrogenase (LADH) with the rho-trifluoromethyl derivatives of benzyl alcohol, benzaldehyde, and benzoic acid have been investigated by use of 19F nuclear mag...

Prochiral selectivity in H(2)O(2)-promoted oxidation of arylalkanols catalysed by chloroperoxidase. The role of the interactions between the OH group and the amino-acid residues in the enzyme active site.

Eur. J. Biochem. 268(3) , 665-72, (2001)

The H(2)O(2)-promoted oxidations of (R)-[alpha-(2)H(1)]-and (S)-[alpha-(2)H(1)]-arylalkanols catalysed by chloroperoxidase (CPO) from Caldariomyces fumago have been investigated. It has been found tha...

J. Chem. Soc., Perkin Trans. II , 1145, (1992)

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