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1-amino-3,3,4,4,5,5,5-heptafluoropentan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

336-53-8

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336-53-8 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 5 carbon (C), 1 hydrogen (H), 7 fluorine (F), 1 nitrogen (N), and 1 oxygen (O) atoms.

Explanation

The compound contains a primary amino group (-NH2) and a hydroxyl group (-OH), which contribute to its chemical reactivity and properties.

Explanation

The presence of a hydroxyl group (-OH) in the molecule classifies it as an alcohol.

Explanation

The compound is an aminoalcohol due to the presence of both a primary amino group and a hydroxyl group in its structure.

Explanation

1-amino-3,3,4,4,5,5,5-heptafluoropentan-2-ol is used as a starting material or intermediate in the synthesis of various pharmaceuticals and agrochemicals.

Explanation

The compound's unique properties make it a valuable reagent and starting material for the synthesis of other fluorinated organic compounds and in various organic chemistry reactions.

Explanation

The presence of seven fluorine atoms in the molecule contributes to its unique properties, such as increased lipophilicity, stability, and reactivity.

Explanation

The chemical reactivity of 1-amino-3,3,4,4,5,5,5-heptafluoropentan-2-ol is affected by its fluorination and the presence of both a primary amino group and a hydroxyl group, which can participate in various chemical reactions.

Explanation

The physical properties of the compound, such as solubility, boiling point, and melting point, are influenced by its highly fluorinated nature and the presence of polar functional groups.

Explanation

The presence of fluorine atoms in the molecule increases its stability, making it more resistant to degradation and chemical reactions under certain conditions.

Functional groups

Primary amino group and hydroxyl group

Fluorinated alcohol

Contains a hydroxyl group

Aminoalcohol

Contains both an amino group and a hydroxyl group

Application

Building block in pharmaceuticals and agrochemicals

Potential applications

Synthesis of fluorinated organic compounds and as a reagent in organic chemistry

Highly fluorinated molecule

Contains seven fluorine atoms

Chemical reactivity

Influenced by fluorination and functional groups

Physical properties

Influenced by fluorination and molecular structure

Stability

Enhanced due to fluorination

Check Digit Verification of cas no

The CAS Registry Mumber 336-53-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 336-53:
(5*3)+(4*3)+(3*6)+(2*5)+(1*3)=58
58 % 10 = 8
So 336-53-8 is a valid CAS Registry Number.

336-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-3,3,4,4,5,5,5-heptafluoropentan-2-ol

1.2 Other means of identification

Product number -
Other names 1-Amino-3,3,4,4,5,5,5-heptafluor-pentan-2-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:336-53-8 SDS

336-53-8Downstream Products

336-53-8Relevant academic research and scientific papers

The synthesis of fluorine-containing pterins

Dunn, Caroline,Gibson, Colin L.,Suckling, Colin J.

, p. 13017 - 13026 (2007/10/03)

The synthesis of some 7,7-difluoro-7,8-dihydropterins and pterins with fluoroalkyl substituents at the 6 or 7 positions from fluorine-containing aliphatic precursors and suitably substituted pyrimidines is described. The fluorine-containing pterins were found to be very insoluble and also stable to nucleophiles and bases in dilute aqueous solution.

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