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2,2,3,3-Tetramethylaziridine is an organic compound with the chemical formula C6H13N. It is a colorless liquid that is soluble in water and has a molecular weight of 99.18 g/mol. This cyclic amine is known for its high reactivity due to the presence of a strained three-membered ring, which makes it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also used as a reagent in organic synthesis, particularly for the preparation of aziridines and other nitrogen-containing compounds. Due to its reactivity, it is important to handle 2,2,3,3-Tetramethylaziridine with care, as it can be hazardous and may have potential health risks.

5910-14-5

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5910-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5910-14-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,1 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5910-14:
(6*5)+(5*9)+(4*1)+(3*0)+(2*1)+(1*4)=85
85 % 10 = 5
So 5910-14-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H13N/c1-5(2)6(3,4)7-5/h7H,1-4H3

5910-14-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3-Tetramethylaziridine

1.2 Other means of identification

Product number -
Other names Aziridine,2,2,3,3-tetramethyl

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:5910-14-5 SDS

5910-14-5Relevant academic research and scientific papers

Direct aziridination of alkenes by a cationic (Salen)ruthenium(VI) nitrido complex

Man, Wai-Lun,Lam, William W. Y.,Yiu, Shek-Man,Lau, Tai-Chu,Peng, Shie-Ming

, p. 15336 - 15337 (2004)

[RuVI(N)(salchda)(CH3OH)]PF6 (1) (salchda = N,N′-bis(salicylidene)o-cyclohexyldiamine dianion) reacts readily with 2,3-dimethyl-2-butene at room temperature in the presence of pyridine or 1-methylimidazole to give initially [RuVI(Az1(-H))(salchda)(py)]PF6 (2, Az1 = 2,2,3,3-tetramethylaziridine), which is then slowly reduced to [RuIII(Az1)(salchda)(py)]PF6 (3). 1 also reacts with a variety of aryl-substituted alkenes such as styrene and trans-β-methylstyrene in the presence of py or 1-MeIm to give the corresponding ruthenium(III) aziridine complexes. The structures of 3 and [RuIII(Az2)(salchda)(1-MeIm)]PF6 (4, Az2 = trans-2-methyl-3-phenylaziridine) have been determined by X-ray crystallography. The Ru-N(aziridine) distances (2.1049, 2.097 A) are consistent with a neutral aziridine ligand. The C-C and C-N distances in the aziridine ligands are all indicative of single bonds. Copyright

Transformation of 1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole derivatives into isoxazoles

Chukanov,Popov,Romanenko,Reznikova

, p. 1227 - 1233 (2008/09/19)

The reactions of 1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole derivatives with electrophilic reagents, such as protic acids, benzoyl chloride, BF 3, and bromine, produce isoxazole, 2,2,3,3-tetramethylaziridine, and 2,3,3-trimethylpropen-2-ylamine

CHIMIE DES RADIOPROTECTEURS : II. SYNTHESE DE NOUVEAUX ACIDES S-(AMINOETHYL-2) PHOSPHOROTHIOIQUES SUBSTITUES

Lion, Claude,Boukou-Poba, Jean-Paul,Saumtally, Imran

, p. 711 - 718 (2007/10/02)

A new method for the synthesis of biologically interesting substituted S(2-aminoethyl) phosphorothioic acids H2NCR1R2-CR3R4SPO3H2 is described.It employs the sequence : olefine R1R2C=CR3R4 - α-bromoazide N3R1R2C-CBrR3R4 - aziridine or α-bromamin

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