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Ethene, 1-fluoro-2-iodo-, (E)-, also known as (E)-1-fluoro-2-iodoethane or (E)-1,2-dihaloethane, is an organic compound with the chemical formula C2H3FI. It is a halogenated derivative of ethene, featuring a fluorine atom at the first carbon and an iodine atom at the second carbon, with the double bond between the two carbons. Ethene, 1-fluoro-2-iodo-, (E)- is a colorless liquid with a pungent odor and is sensitive to light and heat. It is used in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Due to its reactivity, it is typically handled under controlled conditions to prevent unwanted side reactions.

2353-82-4

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2353-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2353-82-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2353-82:
(6*2)+(5*3)+(4*5)+(3*3)+(2*8)+(1*2)=74
74 % 10 = 4
So 2353-82-4 is a valid CAS Registry Number.

2353-82-4SDS

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-fluoro-2-iodoethene

1.2 Other means of identification

Product number -
Other names trans-1-fluoro-2-iodoethylene

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:2353-82-4 SDS

2353-82-4Upstream product

2353-82-4Downstream Products

2353-82-4Relevant academic research and scientific papers

Efficient microscale preparation of isotopically enriched 1-[ 79Br]bromo-2-fluoroethylene, [79Br]BrHC=CHF

Baldan, Alessandro,Tassan, Augusto

, p. 1447 - 1453 (2007/10/03)

An efficient preparation of 1-[79Br]bromo-2-fliioroethylene, [79Br]BrHC= CHF, was carried out by a three-step procedure: (a) natural 1-bromo-2-fluoroethylene, BrHC=CHF, was iodinated to 1-fluoro-2-iodoethylene, FHC=CHI; (b) 1-fluoro-2-iodoethylene was 79Br2-brominated to 1,2-di[79Br]bromo-1-fluoro- 2-iodoethane, [79Br]BrFCHCH[79Br]BrI; and (c) 1,2-di[ 79Br]bromo-1-fluoro-2-iodoethane was dehalogenated to 1-[ 79Br]bromo-2-fluoroethylene, [79Br]BrHC=CHF. The yield of isolated product, on a 2-mmol scale, was 62% with respect to 79Br2. Copyright Taylor & Francis, Inc.

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