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1737-28-6

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1737-28-6 Usage

General Description

1-[4-(Trifluoromethoxy)phenyl]ethan-1-ol, also known as 4-(Trifluoromethoxy)phenethyl alcohol, is an organic compound with the chemical formula C9H9F3O2. It is a colorless liquid that is commonly used as a synthetic intermediate in the production of pharmaceuticals and agrochemicals. 1-[4-(TRIFLUOROMETHOXY)PHENYL]ETHAN-1-OL is also used as a solvent and a reagent in organic synthesis. Its structure contains a phenyl ring with a trifluoromethoxy group substituted at the 4-position and an ethyl group attached to the phenyl ring at the 1-position. 1-[4-(Trifluoromethoxy)phenyl]ethan-1-ol has applications in various industries, including pharmaceuticals, agrochemicals, and organic synthesis, making it a versatile and important chemical compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1737-28-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1737-28:
(6*1)+(5*7)+(4*3)+(3*7)+(2*2)+(1*8)=86
86 % 10 = 6
So 1737-28-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9F3O2/c1-6(13)7-2-4-8(5-3-7)14-9(10,11)12/h2-6,13H,1H3

1737-28-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H31561)  1-[4-(Trifluoromethoxy)phenyl]ethanol, 97%   

  • 1737-28-6

  • 5g

  • 471.0CNY

  • Detail
  • Alfa Aesar

  • (H31561)  1-[4-(Trifluoromethoxy)phenyl]ethanol, 97%   

  • 1737-28-6

  • 25g

  • 1566.0CNY

  • Detail

1737-28-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-(trifluoromethoxy)phenyl]ethanol

1.2 Other means of identification

Product number -
Other names 1-(4-Trifluoromethoxyphenyl)ethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1737-28-6 SDS

1737-28-6Relevant articles and documents

Method for synthesizing secondary alcohol in water phase

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Paragraph 0033-0034, (2021/07/14)

The invention discloses a method for synthesizing secondary alcohol in a water phase. The method comprises the following steps: taking ketone as a raw material, selecting water as a solvent, and carrying out catalytic hydrogenation reaction on the ketone in the presence of a water-soluble catalyst to obtain the secondary alcohol, wherein the catalyst is a metal iridium complex [Cp * Ir (2, 2'-bpyO)(OH)][Na]. Water is used as the solvent, so that the use of an organic solvent is avoided, and the method is more environment-friendly; the reaction is carried out at relatively low temperature and normal pressure, and the reaction conditions are mild; alkali is not needed in the reaction, so that generation of byproducts is avoided; and the conversion rate of the raw materials is high, and the yield of the obtained product is high. The method not only has academic research value, but also has a certain industrialization prospect.

RETRACTED ARTICLE: The Manganese(I)-Catalyzed Asymmetric Transfer Hydrogenation of Ketones: Disclosing the Macrocylic Privilege

Passera, Alessandro,Mezzetti, Antonio

supporting information, p. 187 - 191 (2019/12/11)

The bis(carbonyl) manganese(I) complex [Mn(CO)2(1)]Br (2) with a chiral (NH)2P2 macrocyclic ligand (1) catalyzes the asymmetric transfer hydrogenation of polar double bonds with 2-propanol as the hydrogen source. Ketones (43 substrates) are reduced to alcohols in high yields (up to >99 %) and with excellent enantioselectivities (90–99 % ee). A stereochemical model based on attractive CH–π interactions is proposed.

NOVEL SPIROPIPERIDINE PROLYLCARBOXYPEPTIDASE INHIBITORS

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Page/Page column 54-55, (2011/11/13)

Compounds of structural formula (I) are inhibitors of prolylcarboxypeptidase (PrCP). The compounds of the present invention are useful for the prevention and treatment of conditions related to enzymatic activity of PrCP such as abnormal metabolism, including obesity; diabetes; metabolic syndrome; obesity related disorders; and diabetes related disorders.

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