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57308-89-1

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57308-89-1 Usage

Type of compound

Heterocyclic compound with a thiophene ring

Substituents

Chlorine and iodine

Uses

Organic synthesis, building block for various organic compounds, production of pharmaceuticals and agrochemicals

Unique properties

Electronic and optical properties

Safety precautions

Potential health hazards and environmental impact, proper safety measures required

Check Digit Verification of cas no

The CAS Registry Mumber 57308-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,0 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57308-89:
(7*5)+(6*7)+(5*3)+(4*0)+(3*8)+(2*8)+(1*9)=141
141 % 10 = 1
So 57308-89-1 is a valid CAS Registry Number.

57308-89-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dichloro-3,4-diiodothiophene

1.2 Other means of identification

Product number -
Other names 2,5-dichloro-3,4-diiodo-thiophene

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:57308-89-1 SDS

57308-89-1Upstream product

57308-89-1Relevant articles and documents

EPR investigations of β-deuteriated 5,5"-dimethyl-2,2':5',2"-terthiophenes

Engelmann, Guennar,Stoesser, Reinhard,Kossmehl, Gerhard,Jugelt, Werner,Welzel, Hans-Peter

, p. 2015 - 2020 (2007/10/03)

The unambiguous assignment of the β-hyperfine coupling constants of the radical cations of 5,5"-dimethyl-2,2':5',2"-terthiophene (11) has been achieved by EPR spectroscopic investigations of the deuteriated compounds 12, 13, and 14.The syntheses of these substances were achieved by cross-coupling following the Negishi and Kumada reaction starting from deuteriated derivatives of chloromethylated thiophene derivatives.The generation of the radical cations was carried out by electrochemical oxidation at a constant potential in the EPR spectrometr.In the presence of acidic compounds a D-H exchange at the β-positions of oligothiophenes was observed.The experimentally determined spin density distribution was rationalized by means of semiempirical quantum mechanical calculations (RHF-INDO-SP).Theoretical and experimental assignments are in good agreement.

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