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Benzeneethanol, 3-fluoro-beta-methylene- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 195528-43-9 Structure
  • Basic information

    1. Product Name: Benzeneethanol, 3-fluoro-beta-methylene- (9CI)
    2. Synonyms: Benzeneethanol, 3-fluoro-beta-methylene- (9CI)
    3. CAS NO:195528-43-9
    4. Molecular Formula: C9H9FO
    5. Molecular Weight: 152.1655632
    6. EINECS: N/A
    7. Product Categories: HALIDE
    8. Mol File: 195528-43-9.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: Benzeneethanol, 3-fluoro-beta-methylene- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzeneethanol, 3-fluoro-beta-methylene- (9CI)(195528-43-9)
    11. EPA Substance Registry System: Benzeneethanol, 3-fluoro-beta-methylene- (9CI)(195528-43-9)
  • 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: 195528-43-9(Hazardous Substances Data)

195528-43-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 195528-43-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,5,2 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 195528-43:
(8*1)+(7*9)+(6*5)+(5*5)+(4*2)+(3*8)+(2*4)+(1*3)=169
169 % 10 = 9
So 195528-43-9 is a valid CAS Registry Number.

195528-43-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-fluorophenyl)prop-2-en-1-ol

1.2 Other means of identification

Product number -
Other names 2-(3-fluorophenyl)-2-propen-1-ol

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:195528-43-9 SDS

195528-43-9Relevant articles and documents

Copper-Catalyzed Asymmetric Hydroallylation of Vinylsilanes

Guo, Xiaobing,Niu, Junbo,Wang, Simin,Xiong, Tao,Zhang, Qian,Zhang, Qiao

supporting information, (2022/02/21)

A copper-catalyzed asymmetric hydroallylation of readily available vinylsilanes with allylic phosphates in the presence of hydrosilane was developed. These transformations can be performed under mild reaction conditions and provide the useful chiral organ

Nickel-catalyzed enantioselective hydrovinylation of silyl-protected allylic alcohols: An efficient access to homoallylic alcohols with a chiral quaternary center

Zhang, Qi,Zhu, Shou-Fei,Cai, Yan,Wang, Li-Xin,Zhou, Qi-Lin

experimental part, p. 1899 - 1906 (2011/02/25)

Asymmetric hydrovinylation of silyl-protected allylic alcohols catalyzed by nickel complexes of chiral spiro phosphoramidite ligands was developed. A series of homoallylic alcohols with a chiral quaternary center were produced in high yields (up to 97%) and high enantioselectivities (up to 95% ee). The reaction provides an efficient method for preparing bifunctional compounds with a chiral quaternary carbon center.

Regioselective Heck arylation of unsaturated alcohols by palladium catalysis in ionic liquid

Mo, Jun,Xu, Lijin,Ruan, Jiwu,Liu, Shifang,Xiao, Jianliang

, p. 3591 - 3593 (2008/09/20)

In contrast to almost all of the known examples of Heck arylation of unsaturated alcohols, which yield predominately β-arylated products, arylation under the Pd-DPPP catalysis in ionic liquid leads preferentially to aryl substitution at the α carbon, prov

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