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3-Fluoro-5-(trifluoromethyl)phenyl isocyanate, also known as 1-fluoro-3-isocyanato-5-(trifluoromethyl)benzene, is an organic building block that features an isocyanate group. 3-FLUORO-5-(TRIFLUOROMETHYL)PHENYL is characterized by the presence of a fluorine atom at the 3-position and a trifluoromethyl group at the 5-position on a phenyl ring, with an isocyanate functional group attached to the 3-position.

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  • 302912-19-2 Structure
  • Basic information

    1. Product Name: 3-FLUORO-5-(TRIFLUOROMETHYL)PHENYL
    2. Synonyms: 3-FLUORO-5-(TRIFLUOROMETHYL)PHENYL;Benzene, 1-fluoro-3-isocyanato-5-(trifluoromethyl)- (9CI);3-Fluoro-5-(trifluoromethyl)phenyl isocyanate, 97+%;3-Fluoro-5-(trifluoromethyl)phenyl isocyanate 97%
    3. CAS NO:302912-19-2
    4. Molecular Formula: C8H3F4NO
    5. Molecular Weight: 205.11
    6. EINECS: N/A
    7. Product Categories: ISOCYANATE;Isocyanates;Nitrogen Compounds;Organic Building Blocks
    8. Mol File: 302912-19-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 164 °C(lit.)
    3. Flash Point: >230 °F
    4. Appearance: /
    5. Density: 1.423 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 1.33mmHg at 25°C
    7. Refractive Index: n20/D 1.446(lit.)
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-FLUORO-5-(TRIFLUOROMETHYL)PHENYL(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-FLUORO-5-(TRIFLUOROMETHYL)PHENYL(302912-19-2)
    12. EPA Substance Registry System: 3-FLUORO-5-(TRIFLUOROMETHYL)PHENYL(302912-19-2)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 20/21/22-36/37/38-42
    3. Safety Statements: 23-26-36
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 302912-19-2(Hazardous Substances Data)

302912-19-2 Usage

Uses

Used in Pharmaceutical Industry:
3-Fluoro-5-(trifluoromethyl)phenyl isocyanate is used as a reactant for the synthesis of RIP1 kinase inhibitors. These inhibitors are crucial in the treatment of pathologies associated with necroptosis, a form of programmed cell death that occurs in response to various cellular stressors and can contribute to the development of various diseases.
The application of this compound in the pharmaceutical industry is significant due to its role in the development of potential therapeutic agents that can target and modulate the activity of RIP1 kinase, thereby providing a novel approach to treating necroptosis-related conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 302912-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,9,1 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 302912-19:
(8*3)+(7*0)+(6*2)+(5*9)+(4*1)+(3*2)+(2*1)+(1*9)=102
102 % 10 = 2
So 302912-19-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H3F4NO/c9-6-1-5(8(10,11)12)2-7(3-6)13-4-14/h1-3H

302912-19-2 Well-known Company Product Price

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  • Aldrich

  • (495573)  3-Fluoro-5-(trifluoromethyl)phenylisocyanate  97%

  • 302912-19-2

  • 495573-2G

  • 2,703.87CNY

  • Detail

302912-19-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-3-isocyanato-5-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names -

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:302912-19-2 SDS

302912-19-2Relevant articles and documents

GLUCAGON ANTAGONISTS/INVERSE AGONISTS

-

Page/Page column 158, (2010/02/14)

A novel class of compounds, which act to antagonize the action of the glucagon hormone on the glucagon receptor. Owing to their antagonizing effect of the glucagon receptor the compounds may be suitable for the treatment and/or prevention of any glucagon-

Glucagon antagonists/inverse agonists

-

, (2008/06/13)

Disclosed is a novel class of compounds of formula (I) wherein V, A, Y, Z, R1, E, X and D are as defined in the specification. These compounds act to antagonize the action of the glucagon hormone on the glucagon receptor. Owing to their antagonizing effect of the glucagon receptor, the compounds are suitable for treating or preventing glucagon-mediated conditions and diseases such as hyperglycemia, Type 1 diabetes, Type 2 diabetes and obesity.

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