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(S)-(+)-2-(tert-Butyl)-3-methyl-4-imidazolidinone trifluoroacetic acid is a Macmillan imidazolidinone organocatalyst, which is a type of chiral small molecule that plays a crucial role in asymmetric transformation reactions. It is characterized by its unique structure, featuring a tert-butyl group at the 2-position, a methyl group at the 3-position, and a trifluoroacetic acid moiety attached to the imidazolidinone ring. This specific arrangement endows the compound with distinctive properties that make it highly effective in catalyzing a variety of chemical reactions with high enantioselectivity.

900503-70-0

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900503-70-0 Usage

Uses

Used in Pharmaceutical Industry:
(S)-(+)-2-(tert-Butyl)-3-methyl-4-imidazolidinone trifluoroacetic acid is used as a chiral catalyst for the synthesis of enantiomerically pure pharmaceutical compounds. Its ability to induce high enantioselectivity in asymmetric reactions is invaluable in the production of single-enantiomer drugs, which is essential for ensuring the desired therapeutic effects and minimizing potential side effects.
Used in Fine Chemicals Synthesis:
In the fine chemicals industry, (S)-(+)-2-(tert-Butyl)-3-methyl-4-imidazolidinone trifluoroacetic acid is employed as a key organocatalyst for the preparation of enantiomerically pure compounds with high selectivity. This is particularly important in the synthesis of fragrances, flavors, and agrochemicals, where the purity and stereochemistry of the final product can significantly impact their performance and safety.
Used in Academic Research:
(S)-(+)-2-(tert-Butyl)-3-methyl-4-imidazolidinone trifluoroacetic acid is utilized as a research tool in academic settings to study the mechanisms of asymmetric catalysis and to develop new methodologies for enantioselective synthesis. Its unique structural features and catalytic properties make it an attractive candidate for exploring novel reaction pathways and expanding the scope of asymmetric transformations.
Used in Green Chemistry:
(S)-(+)-2-(tert-Butyl)-3-methyl-4-imidazolidinone trifluoroacetic acid is also used in green chemistry initiatives, as its application in asymmetric catalysis can lead to more efficient and environmentally friendly synthetic processes. By enabling the selective formation of desired enantiomers, this organocatalyst can help reduce waste, lower energy consumption, and minimize the use of hazardous materials in chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 900503-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,0,5,0 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 900503-70:
(8*9)+(7*0)+(6*0)+(5*5)+(4*0)+(3*3)+(2*7)+(1*0)=120
120 % 10 = 0
So 900503-70-0 is a valid CAS Registry Number.

900503-70-0 Well-known Company Product Price

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  • Aldrich

  • (661902)  (S)-(+)-2-(tert-Butyl)-3-methyl-4-imidazolidinonetrifluoroaceticacid  96%

  • 900503-70-0

  • 661902-500MG

  • 1,144.26CNY

  • Detail
  • Aldrich

  • (661902)  (S)-(+)-2-(tert-Butyl)-3-methyl-4-imidazolidinonetrifluoroaceticacid  96%

  • 900503-70-0

  • 661902-2G

  • 3,701.88CNY

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900503-70-0SDS

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 (S)-2-(t-butyl)-3-methyl-4-imidazolidinone trifluroacetic acid salt

1.2 Other means of identification

Product number -
Other names (S)-2-tert-butyl-3-methylimidazolidin-4-one trichloroacetate salt

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:900503-70-0 SDS

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