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1-Fluoro-2-heptanone is a colorless liquid organic compound with the chemical formula C7H13FO. It is a derivative of heptanone, where one hydrogen atom is replaced by a fluorine atom. This fluorinated ketone is used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is characterized by its unique reactivity and properties due to the presence of the fluorine atom, which can influence the molecule's polarity, lipophilicity, and reactivity. 1-Fluoro-2-heptanone is typically synthesized through fluorination reactions and is handled with care due to its potential toxicity and reactivity.

689-87-2

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689-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 689-87-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 689-87:
(5*6)+(4*8)+(3*9)+(2*8)+(1*7)=112
112 % 10 = 2
So 689-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H13FO/c1-2-3-4-5-7(9)6-8/h2-6H2,1H3

689-87-2SDS

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 1-fluoroheptan-2-one

1.2 Other means of identification

Product number -
Other names 1-fluoro-2-heptanone

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:689-87-2 SDS

689-87-2Downstream Products

689-87-2Relevant academic research and scientific papers

Synthesis, Regioselective Deprotonation, and Stereoselective Alkylation of Fluoro Ketimines

Welch, John T.,Seper, Karl W.

, p. 2991 - 2999 (2007/10/02)

Fluoroacetone imines of cyclohexylamine, valinol O-methyl ether, and phenylalaninol O-methyl ether and 2-fluorocyclohexanone imines of cyclohexylamine and phenylalaninol O-methyl ether were prepared.The temperature-dependent, regioselective deprotonation of these imines was employed in highly regioselective alkylation reactions.The deprotonation of fluoroacetone cyclohexylimine on the carbon bearing fluorine yielded only a single stereoisomer as determined by low temperature 19F NMR.In contrast, deprotonation of fluoroacetone O-benzyloximes was not regiospecific under any of the conditions examined.

The Temperature-Dependent Regioselective Deprotonation of Fluoroacetone Cyclohexylimine

Welch, John T.,Seper, Karl W.

, p. 119 - 120 (2007/10/02)

The temperature-dependent regioselective deprotonation of fluoroacetone cyclohexylimine was developed as a procedure for the regioselective alkylation of fluoroacetone.

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