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4-Fluorobutyraldehyde is an organic compound with the chemical formula C4H7FO. It is a colorless liquid that is soluble in water and has a pungent odor. This aldehyde is a fluorinated derivative of butyraldehyde, where one of the hydrogen atoms on the fourth carbon is replaced by a fluorine atom. It is used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique reactivity and properties. 4-Fluorobutyraldehyde is also known for its potential applications in the production of fluorinated compounds, which have a wide range of uses in the chemical industry.

462-74-8

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462-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 462-74-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 462-74:
(5*4)+(4*6)+(3*2)+(2*7)+(1*4)=68
68 % 10 = 8
So 462-74-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H7FO/c5-3-1-2-4-6/h4H,1-3H2

462-74-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluorobutanal

1.2 Other means of identification

Product number -
Other names Butanal,4-fluoro

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:462-74-8 SDS

462-74-8Relevant academic research and scientific papers

Racemic thioesters for production of polyketides

-

, (2008/06/13)

Facile methods for preparing diketide and triketide thioesters are disclosed. The resulting thioesters may be used as intermediates in the synthesis of desired polyketides, and may contain functional groups which ultimately reside in side chains on the resulting polyketide and thus can be used further to manipulate the polyketide so as form derivatives. The polyketides produced may also be tailored by glycosylation, hydroxylation and the like. New polyketides and their derivatives and tailored forms are thereby produced.

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