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585-45-5

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585-45-5 Usage

Chemical compound

Epoxide with a trifluoromethyl group and a phenoxy group attached to the oxirane ring

Also known as

Trifenagrel and CVN162

Potential therapeutic effects

Treatment of thrombosis and other cardiovascular conditions

Mechanism of action

Potent and selective antagonist of the platelet P2Y12 receptor

Role in platelet aggregation

Inhibits blood clot formation

Potential application

Development of antithrombotic drugs

Research status

Further evaluation needed for efficacy and safety in clinical use

Check Digit Verification of cas no

The CAS Registry Mumber 585-45-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 585-45:
(5*5)+(4*8)+(3*5)+(2*4)+(1*5)=85
85 % 10 = 5
So 585-45-5 is a valid CAS Registry Number.

585-45-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[3-(trifluoromethyl)phenoxy]methyl]oxirane

1.2 Other means of identification

Product number -
Other names (3-(2,3-Epoxypropoxy)propyl)triethoxysilane

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:585-45-5 SDS

585-45-5Relevant articles and documents

Substituted diaryl compound and preparation method and application thereof

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Paragraph 0073-0075; 0076, (2021/09/15)

The invention relates to the field of medicinal chemistry, in particular to a substituted diaryl compound (I). The preparation method comprises the following steps: medicine preparation and medical application thereof. Test results show that the substituted diaryl compound has a good inhibition effect on human lung cancer (A549), human ovarian cancer (SKOV3), human melanoma (A375) and human colon cancer (LOVO) cells. Formula (I):

Discovery of (phenoxy-2-hydroxypropyl)piperidines as a novel class of voltage-gated sodium channel 1.7 inhibitors

Suzuki, Sayaka,Kuroda, Takeshi,Kimoto, Hiroko,Domon, Yuki,Kubota, Kazufumi,Kitano, Yutaka,Yokoyama, Tomihisa,Shimizugawa, Akiko,Sugita, Ryusuke,Koishi, Ryuta,Asano, Daigo,Tamaki, Kazuhiko,Shinozuka, Tsuyoshi,Kobayashi, Hiroyuki

, p. 5419 - 5423 (2015/11/09)

A novel class of NaV1.7 inhibitors has been identified by high-throughput screening followed by structure activity relationship studies. Among this series of compounds, piperidine 9o showed potent human and mouse NaV1.7 inhibitory activities with fair subtype selectivity over NaV1.5. Compound 9o successfully demonstrated analgesic efficacy in mice comparable to that of the currently used drug, mexiletine, but with an expanded central nervous system safety margin.

ANALGESIC THAT BINDS FILAMIN A

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Page/Page column 114; 115, (2010/05/14)

A compound, composition and method are disclosed that can provide analgesia. A contemplated compound has a structure that corresponds to Formula A, wherein A, B, X, R1, R2, R7 and R8, and the dashed lines are defined within.

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