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688362-77-8

Benzenemethanamine, alpha-ethenyl-4-fluoro-, (alphaR)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 688362-77-8 Structure

  • Basic information

    1. Product Name: Benzenemethanamine, alpha-ethenyl-4-fluoro-, (alphaR)- (9CI)
    2. Synonyms: Benzenemethanamine, alpha-ethenyl-4-fluoro-, (alphaR)- (9CI)
    3. CAS NO:688362-77-8
    4. Molecular Formula: C9H10FN
    5. Molecular Weight: 151.1808032
    6. EINECS: N/A
    7. Product Categories: HALIDE
    8. Mol File: 688362-77-8.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: Benzenemethanamine, alpha-ethenyl-4-fluoro-, (alphaR)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanamine, alpha-ethenyl-4-fluoro-, (alphaR)- (9CI)(688362-77-8)
    11. EPA Substance Registry System: Benzenemethanamine, alpha-ethenyl-4-fluoro-, (alphaR)- (9CI)(688362-77-8)

  • 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: 688362-77-8(Hazardous Substances Data)

688362-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 688362-77-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,8,3,6 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 688362-77:
(8*6)+(7*8)+(6*8)+(5*3)+(4*6)+(3*2)+(2*7)+(1*7)=218
218 % 10 = 8
So 688362-77-8 is a valid CAS Registry Number.

688362-77-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1-(4-fluorophenyl)-2-propenylamine

1.2 Other means of identification

Product number -
Other names (R)-1-(4-Fluoro-phenyl)-allylamine

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:688362-77-8 SDS

688362-77-8Relevant articles and documents

Ruthenium-catalyzed intramolecular hydrocarbamoylation of allylic formamides: Convenient access to chiral pyrrolidones

Armanino, Nicolas,Carreira, Erick M.

supporting information, p. 6814 - 6817 (2013/06/05)

An attractive strategy for the synthesis of saturated nitrogen-containing heterocycles is described herein, involving the implementation of ruthenium-catalyzed intramolecular hydrocarbamoylation of olefins. The process proceeds by formal C-H bond cleavage

Design, synthesis, and SAR of macrocyclic tertiary carbinamine BACE-1 inhibitors

Lindsley, Stacey R.,Moore, Keith P.,Rajapakse, Hemaka A.,Selnick, Harold G.,Young, Mary Beth,Zhu, Hong,Munshi, Sanjeev,Kuo, Lawrence,McGaughey, Georgia B.,Colussi, Dennis,Crouthamel, Ming-Chih,Lai, Ming-Tain,Pietrak, Beth,Price, Eric A.,Sankaranarayanan, Sethu,Simon, Adam J.,Seabrook, Guy R.,Hazuda, Daria J.,Pudvah, Nicole T.,Hochman, Jerome H.,Graham, Samuel L.,Vacca, Joseph P.,Nantermet, Philippe G.

, p. 4057 - 4061 (2008/02/10)

This Letter describes the design and synthesis of tertiary carbinamine macrocyclic inhibitors of the β-secretase (BACE-1) enzyme. These macrocyclic inhibitors, some of which incorporate novel P2 substituents, display a 2- to 100-fold increase in potency r

Enantioselective synthesis of 1-aryl-2-propenylamines: A new approach to a stereoselective synthesis of the Taxol side chain

Castagnolo, Daniele,Armaroli, Silvia,Corelli, Federico,Botta, Maurizio

, p. 941 - 949 (2007/10/03)

A variety of substituted 1-aryl-2-propenylamines of high enantiomeric purity were prepared via lipase-catalysed resolution of the corresponding racemates. (R)-1-Phenyl-2-propenylamine was further synthesised into (2R,3S)-3-benzoylamino-2-hydroxy-3-phenylpropanoic acid methyl ester, the side chain of Taxol.

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