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128008-30-0

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128008-30-0 Usage

Description

Indium(III) trifluoromethanesulfonate, also known as triflate, is an organometallic compound with the chemical formula In(OTf)3. It is an off-white powder or granules and is widely recognized for its catalytic properties in various chemical reactions.

Uses

Used in Organic Synthesis:
Indium(III) trifluoromethanesulfonate is used as a Lewis acid catalyst in organic synthesis, facilitating numerous chemical reactions and improving their efficiency.
Used in Organometallic Catalysis:
In the field of organometallic catalysis, Indium(III) trifluoromethanesulfonate serves as a co-catalyst, enhancing the performance of other catalysts and promoting specific chemical transformations.
Used in the Preparation of Stable Indium Bacteriochlorins:
Indium(III) trifluoromethanesulfonate is utilized as a reactant in the preparation of stable indium bacteriochlorins, which are complex organic compounds with potential applications in various fields.
Used in the Study of Basicities of Phosphoryl Compounds:
INDIUM(III) TRIFLUOROMETHANESULFONATE is also employed in the study of basicities of phosphoryl compounds toward triflates and Lewis acids, providing valuable insights into their reactivity and potential applications.
Used in the Preparation of Decahydroquinoline-Type Toxins:
Indium(III) trifluoromethanesulfonate is used as a reactant in the synthesis of decahydroquinoline-type toxins through intramolecular hetero Diels-Alder reactions, contributing to the development of novel bioactive compounds.
Used in the Synthesis of Benzoxazoles:
In the pharmaceutical industry, Indium(III) trifluoromethanesulfonate is used as a catalyst for the synthesis of benzoxazoles via cyclocondensations, which are important structural motifs in various biologically active molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 128008-30-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,0,0 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 128008-30:
(8*1)+(7*2)+(6*8)+(5*0)+(4*0)+(3*8)+(2*3)+(1*0)=100
100 % 10 = 0
So 128008-30-0 is a valid CAS Registry Number.
InChI:InChI=1/3CHF3O3S.In/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3

128008-30-0 Well-known Company Product Price

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  • Alfa Aesar

  • (40131)  Indium(III) trifluoromethanesulfonate, 99% min   

  • 128008-30-0

  • 10g

  • 1329.0CNY

  • Detail
  • Alfa Aesar

  • (40131)  Indium(III) trifluoromethanesulfonate, 99% min   

  • 128008-30-0

  • 50g

  • 5649.0CNY

  • Detail
  • Aldrich

  • (442151)  Indium(III)trifluoromethanesulfonate  

  • 128008-30-0

  • 442151-5G

  • 810.81CNY

  • Detail
  • Aldrich

  • (442151)  Indium(III)trifluoromethanesulfonate  

  • 128008-30-0

  • 442151-25G

  • 3,322.80CNY

  • Detail

128008-30-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Indium(III) trifluoromethanesulfonate

1.2 Other means of identification

Product number -
Other names Indium Trifluoromethanesulfonate

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:128008-30-0 SDS

128008-30-0Upstream product

128008-30-0Downstream Products

128008-30-0Related news

Intramolecular Diels–Alder reaction of 1,7,9-decatrienoates catalyzed by indium(III) trifluoromethanesulfonate in aqueous media08/22/2019

The intramolecular Diels–Alder reaction of ester-tethered 1,7,9-decatrienoate derivatives in a mixture of water and 2-propanol was catalyzed by indium(III) triflate to give the cycloadducts in good yield with perfect endo-selectivity.detailed

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