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53841-59-1

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53841-59-1 Usage

Color

Colorless (lacking color)

Physical state

Liquid (the compound is in a liquid state at room temperature)

Common uses

Monomer in the production of specialty polymers and elastomers (used as a starting material to create larger, more complex molecules)

Properties

Heat resistance and weatherability (the compound can withstand high temperatures and exposure to the elements without breaking down)

Additional uses

Reagent in organic synthesis and building block in the production of fluorinated materials (used as a reactant or intermediate in the creation of other chemical compounds)

Safety precautions

Flammable and can cause irritation to the skin, eyes, and respiratory system (it is important to handle this compound with care to avoid potential hazards)

Check Digit Verification of cas no

The CAS Registry Mumber 53841-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,4 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53841-59:
(7*5)+(6*3)+(5*8)+(4*4)+(3*1)+(2*5)+(1*9)=131
131 % 10 = 1
So 53841-59-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H9F5OSi/c1-13(2,3)12-4(5(7)8)6(9,10)11/h1-3H3

53841-59-1SDS

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 trimethyl(1,1,3,3,3-pentafluoroprop-1-en-2-yloxy)silane

1.2 Other means of identification

Product number -
Other names 2-Trimethylsiloxyperfluorpropen

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:53841-59-1 SDS

53841-59-1Downstream Products

53841-59-1Relevant articles and documents

One-pot synthesis of 3-fluoro-4-(trifluoromethyl)quinolines from pentafluoropropen-2-ol and their molecular modification

Hosokawa, Tsuyoshi,Matsumura, Akemi,Katagiri, Toshimasa,Uneyama, Kenji

, p. 1468 - 1474 (2008/09/16)

(Chemical Equation Presented) Pentafluoropropen-2-ol (PFP) was prepared by the reaction of hexafluoroacetone (HFA) with Mg/TMSCl. The one-pot tandem sequential reactions of PFP via Mannich addition with aldimines followed by Friedel-Crafts cyclization and aromatization afforded the title quinolines. A variety of corresponding 3-substituted quinolines were derived from the title quinoline by nucleophilic substitution of 3-fluorine with nucleophiles. A defluorinative transformation of the 4-trifluoromethyl group of the title quinoline with hydrazine afforded py razoloquinoline.

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