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304882-57-3

3-fluoro-N-(2-phenylethyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 304882-57-3 Structure

  • Basic information

    1. Product Name: 3-fluoro-N-(2-phenylethyl)benzamide
    2. Synonyms: 3-fluoro-N-(2-phenylethyl)benzamide
    3. CAS NO:304882-57-3
    4. Molecular Formula: C15H14FNO
    5. Molecular Weight: 243.2761632
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 304882-57-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-fluoro-N-(2-phenylethyl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-fluoro-N-(2-phenylethyl)benzamide(304882-57-3)
    11. EPA Substance Registry System: 3-fluoro-N-(2-phenylethyl)benzamide(304882-57-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 304882-57-3(Hazardous Substances Data)

304882-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 304882-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,8,8 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 304882-57:
(8*3)+(7*0)+(6*4)+(5*8)+(4*8)+(3*2)+(2*5)+(1*7)=143
143 % 10 = 3
So 304882-57-3 is a valid CAS Registry Number.

304882-57-3SDS

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 3-fluoro-N-(2-phenylethyl)benzamide

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:304882-57-3 SDS

304882-57-3Relevant articles and documents

Discovery of quinuclidine modulators of cellular progranulin

Burnett, Duane A.,Chen, Angela Y.-P.,Koenig, Gerhard,Lanter, James C.,Williamson, Toni,Blain, Jean-Fran?ois

, (2021/06/30)

Phenotypic screening of an annotated small molecule library identified the quinuclidine tetrahydroisoquinoline solifenacin (1) as a robust enhancer of progranulin secretion with single digit micromolar potency in a murine microglial (BV-2) cell line. Subsequent SAR development led to the identification of 29 with a 38-fold decrease in muscarinic receptor antagonist activity and a 10-fold improvement in BV-2 potency.

Josiphos-Type Binaphane Ligands for Iridium-Catalyzed Enantioselective Hydrogenation of 1-Aryl-Substituted Dihydroisoquinolines

Nie, Huifang,Zhu, Yupu,Hu, Xiaomu,Wei, Zhao,Yao, Lin,Zhou, Gang,Wang, Pingan,Jiang, Ru,Zhang, Shengyong

supporting information, p. 8641 - 8645 (2019/10/17)

Convenient synthesis and useful application of a series of Josiphos-type binaphane ligands were described. The iridium complexes of these chiral diphosphines displayed excellent enantioselectivity and good reactivity in the asymmetric hydrogenation of challenging 1-aryl-substituted dihydroisoquinoline substrates (full conversions, up to >99% ee, 4000 TON). The use of 40% HBr (aqueous solution) as an additive dramatically improved the asymmetric induction of these catalysts. This transformation provided a highly efficient and enantioselective access to chiral 1-aryl-substituted tetrahydroisoquinolines, which were of great importance and common in natural products and biologically active molecules.

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