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N-[3-(Trimethylsilyl)-2-propynyl]phthalimide is an organic compound characterized by its white to yellow to tan solid appearance, which can be found in the form of powder, crystals, crystalline powder, and/or chunks. It is a derivative of phthalimide with a trimethylsilyl group attached to a propynyl moiety, which may contribute to its unique chemical properties and potential applications.

351029-12-4

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351029-12-4 Usage

Uses

Used in Chemical Synthesis:
N-[3-(Trimethylsilyl)-2-propynyl]phthalimide is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows for further functionalization and modification, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Material Science:
In the field of material science, N-[3-(Trimethylsilyl)-2-propynyl]phthalimide is used as a component in the development of advanced materials with specific properties. Its incorporation into polymers, for example, can lead to materials with improved thermal stability, mechanical strength, or optical characteristics.
Used in Pharmaceutical Industry:
N-[3-(Trimethylsilyl)-2-propynyl]phthalimide is used as a potential therapeutic agent in the pharmaceutical industry. Its unique chemical structure may offer novel mechanisms of action or selectivity towards specific biological targets, making it a promising candidate for the development of new drugs to treat various diseases.
Used in Analytical Chemistry:
In analytical chemistry, N-[3-(Trimethylsilyl)-2-propynyl]phthalimide can be employed as a reagent or a derivatizing agent for the analysis of various compounds. Its distinct chemical properties may enable the selective detection or quantification of target analytes in complex samples.
Used in Research and Development:
N-[3-(Trimethylsilyl)-2-propynyl]phthalimide is also used as a research tool in academic and industrial laboratories. Its unique structure and properties make it an interesting subject for studying fundamental chemical reactions, exploring new synthetic methodologies, or investigating the properties of novel materials.

Check Digit Verification of cas no

The CAS Registry Mumber 351029-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,0,2 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 351029-12:
(8*3)+(7*5)+(6*1)+(5*0)+(4*2)+(3*9)+(2*1)+(1*2)=104
104 % 10 = 4
So 351029-12-4 is a valid CAS Registry Number.

351029-12-4 Well-known Company Product Price

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  • Aldrich

  • (699519)  N-[3-(Trimethylsilyl)-2-propynyl]phthalimide  97%

  • 351029-12-4

  • 699519-1G

  • 1,050.66CNY

  • Detail

351029-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-trimethylsilylprop-2-ynyl)isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 1-Phthalimido-3-(trimethylsilyl)propyne

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:351029-12-4 SDS

351029-12-4Downstream Products

351029-12-4Relevant academic research and scientific papers

Synthesis of Acylborons by Ozonolysis of Alkenylboronates: Preparation of an Enantioenriched Amino Acid Acylboronate

Taguchi, Jumpei,Ikeda, Toshiki,Takahashi, Rina,Sasaki, Ikuo,Ogasawara, Yasushi,Dairi, Tohru,Kato, Naoya,Yamamoto, Yasunori,Bode, Jeffrey W.,Ito, Hajime

supporting information, p. 13847 - 13851 (2017/10/12)

A concise synthesis of acylborons was achieved by ozonolysis of alkenyl MIDA (N-methyliminodiacetic acid) boronates. This reaction exhibits excellent functional-group tolerance and is applicable to various acyl MIDA boronates and potassium acyltriflurobor

Efficient synthesis of nevirapine analogs to study its metabolic profile by click fishing

Bernard, Sylvain,Defoy, Daniel,Dory, Yves L.,Klarskov, Klaus

supporting information; experimental part, p. 6127 - 6130 (2010/06/13)

Knowledge of the biotransformation and pharmacokinetics of the antiretroviral agent nevirapine is still insufficient. In order to trace rash inducing metabolites of nevirapine, we devised a short and efficient multi-gram synthesis of a nevirapine analog that can be coupled to azide containing compounds by click chemistry.

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