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Phenol, 2-fluoro-6-(2-propenyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69318-23-6 Structure
  • Basic information

    1. Product Name: Phenol, 2-fluoro-6-(2-propenyl)- (9CI)
    2. Synonyms: Phenol, 2-fluoro-6-(2-propenyl)- (9CI)
    3. CAS NO:69318-23-6
    4. Molecular Formula: C9H9FO
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69318-23-6.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: Phenol, 2-fluoro-6-(2-propenyl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenol, 2-fluoro-6-(2-propenyl)- (9CI)(69318-23-6)
    11. EPA Substance Registry System: Phenol, 2-fluoro-6-(2-propenyl)- (9CI)(69318-23-6)
  • 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: 69318-23-6(Hazardous Substances Data)

69318-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69318-23-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,1 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69318-23:
(7*6)+(6*9)+(5*3)+(4*1)+(3*8)+(2*2)+(1*3)=146
146 % 10 = 6
So 69318-23-6 is a valid CAS Registry Number.

69318-23-6Downstream Products

69318-23-6Relevant articles and documents

Subsupercritical Water Generated by Inductive Heating Inside Flow Reactors Facilitates the Claisen Rearrangement

Oltmanns, Mona,Kirschning, Andreas

supporting information, p. 1942 - 1946 (2020/11/13)

Claisen rearrangement of electron-deficient O-allylated phenols, including fluorine-modified phenols, is facilitated in aqueous media at high temperatures and pressures under flow conditions, as opposed to organic solvents. The O-allylation of phenols can be coupled with the Claisen rearrangement in an integrated flow system.

C- ARYL GLYCOSID DERIVATIVES, PHARMACEUTICAL COMPOSITION, PREPARATION PROCESS AND USES THEREOF

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Paragraph 0191; 0193, (2017/04/19)

This invention relates to a kind of C-aryl glycoside derivatives, its pharmaceutical compositions, preparation methods, and uses thereof. The preparation method comprises: method 1: in a solvent, deprotecting the acetyl protecting groups of compound 1-f in the presence of a base; method 2: 1) compound 2-g reacts with via Mitsunobu reaction; 2) deprotecting the acetyl protecting groups of compound 2-f obtained from step 1; method 3: 1) compound 2-g reacts with via nucleophilic substitution reaction; 2) deprotecting the acetyl protecting groups of compound 3-f obtained from step 1. The pharmaceutical composition comprises a kind of C-aryl glycoside derivatives; it's pharmaceutically acceptable salts and/or prodrugs thereof and excipient thereof. This invention further relates to a kind of C-aryl glycoside derivatives, it's pharmaceutically acceptable salts or pharmaceutical compositions thereof for the use in preparation of a SGLT inhibitor. The C-aryl glycoside derivatives of this invention provides a new direction for the study of SGLT inhibitors.

2 - fluoro - 4 - allyl - 6 - nitro-phenol with 2 - fluoro - 4 - nitro - 6 - allyl phenol joint preparation and use

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Paragraph 0006; 0012, (2017/10/06)

Disclosed are a combined preparation method and an application of 2-fluoro-4-allyl-6-nitrophenol and 2-fluoro-4-nitro-6-allyl phenol. The combined preparation method comprises the steps: with 2-fluorophenyl allyl ether as a raw material, carrying out Clai

Synthesis and pharmacological evaluation of 2-(1-alkylpiperidin-4-yl)-N- [(1R)-1-(4-fluorophenyl)-2-methylpropyl]acetamide derivatives as novel antihypertensive agents

Watanuki, Susumu,Matsuura, Keisuke,Tomura, Yuichi,Okada, Minoru,Okazaki, Toshio,Ohta, Mitsuaki,Tsukamoto, Shin-Ichi

experimental part, p. 223 - 234 (2012/03/11)

We synthesized and evaluated the inhibitory activity of a series of 2-(1-alkylpiperidin-4-yl)-N-[(1R)-1-(4-fluorophenyl)-2-methylpropyl]acetamide derivatives against T-type Ca2+ channels. Structure-activity relationship studies revealed that th

IMPROVED PROCESS FOR THE PREPARATION OF HALO-DIALKOXYBENZENES

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Page/Page column 8-9, (2011/06/23)

The invention describes an improved method for producing halo-dialkoxybenzenes of formula (I) such as 1-fluoro-2, 3-dialkoxybenzene as well as 2-fluoro-1, 4-dialkoxybenzene, Formula (I) by reacting commercial 2-fluorophenol is reacted with an allyl halide

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