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(Trimethylsilyl)imidazole

(Trimethylsilyl)imidazole structure

(Trimethylsilyl)imidazole 

structure
  • CAS No:

    18156-74-6

  • Formula:

    C6H12N2Si

  • Chemical Name:

    (Trimethylsilyl)imidazole

  • Synonyms:

    1H-Imidazole,1-(trimethylsilyl)-;Imidazole,1-(trimethylsilyl)-;1-(Trimethylsilyl)-1H-imidazole;N-(Trimethylsilyl)imidazole;(Trimethylsilyl)imidazole;N-(Trimethylsilyl)imidazol;1-(Trimethylsilyl)imidazole;TSIM;1-Imidazolyltrimethylsilane;Trimethylimidazosilane;TMSI;NSC 139860;N-(Trimethylsilyl)-1H-imidazole;150059-66-8

  • Categories:

    Chemical Reagents  >  Silane Reagent

Description

Colorless transparent liquidChEBI: A member of the class of imidazoles in which the hydrogen at position 1 is replaced by a trimethylsilyl group. N-trimethylsilylimidazole is a derivatisation agent used in gas chromatography/mass spectrometry applications.


N-trimethylsilylimidazole is a member of the class of imidazoles in which the hydrogen at position 1 is replaced by a trimethylsilyl group. N-trimethylsilylimidazole is a derivatisation agent used in gas chromatography/mass spectrometry applications. It has a role as a chromatographic reagent. It is a member of imidazoles and a N-silyl compound.

(Trimethylsilyl)imidazole Basic Attributes

140.26

140.26

606148

242-040-3

139860

DTXSID5066326

29332990

Characteristics

17.8

Clear colorless to yellow Liquid

0.956 g/cm3

105-106 °C

99 °C @ Press: 14 Torr

42 °F

n 20/D 1.475(lit.)

Decomposes in water

2-8°C

Safety Information

II

3

UN 1993 3/PG 2

3

11-36/37/38-14-40-34-37-35-20/21/22

16-26-33-37/39-45-36/37/39

NI8700000

F,Xi,C

P210-P261-P305 + P351 + P338

H225-H315-H319-H335

|Danger|H225 (59.04%): Highly Flammable liquid and vapor [Danger Flammable liquids]|P201, P202, P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P273, P280, P281, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P308+P313, P310, P312, P321, P330, P332+P313, P337+P313, P362, P363, P370+P378, P391, P403+P233, P403+P235, P405, and P501|Aggregated GHS information provided by 83 companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

1-(trimethylsilyl)-1H-imidazole

(Trimethylsilyl)imidazole Use and Manufacturing

Uses

Used as an antibiotic intermediate and a strong silanizing agent; high-efficiency silanizing reagent, especially suitable for the synthesis of alcohols and acyl imidazoles, protecting the hydroxyl group in the presence of amino groups. Antibiotic intermediates. It is an important intermediate for the synthesis of various acylimidazoles, and also an important intermediate for the synthesis of pyrveramide; under the condition of amine functionalization, a silylation reagent that protects the hydroxyl group; a powerful silylation reagent, especially for alcohols; acylimidazole Synthesis of morpholino

1H-Imidazole, 1-(trimethylsilyl)-: ACTIVE

Computed Properties

Molecular Weight:140.26
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:140.076974926
Monoisotopic Mass:140.076974926
Topological Polar Surface Area:17.8
Heavy Atom Count:9
Complexity:97.7
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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