14387-89-4

• 

• Basic information

  1. Product Name: 1,3-Ditert-butylaziridine-2-one
  2. Synonyms: 1,3-Di-tert-butylaziridin-2-one;1,3-Ditert-butylaziridine-2-one
  3. CAS NO:14387-89-4
  4. Molecular Formula: C₁₀H₁₉NO
  5. Molecular Weight: 169.26
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 14387-89-4.mol
  9. Article Data: 5

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 196.1°C at 760 mmHg
  3. Flash Point: 66.6°C
  4. Appearance: /
  5. Density: 0.976g/cm³
  6. Vapor Pressure: 0.405mmHg at 25°C
  7. Refractive Index: 1.48
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 1,3-Ditert-butylaziridine-2-one(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1,3-Ditert-butylaziridine-2-one(14387-89-4)
  12. EPA Substance Registry System: 1,3-Ditert-butylaziridine-2-one(14387-89-4)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 14387-89-4(Hazardous Substances Data)

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• 2-Aziridinone,1,3-bis(1,1-dimethylethyl)-

  Cas No: 14387-89-4

• USD $ 3.0-3.0 / Kilogram

• 1 Kilogram

• 1-100 Metric Ton/Month

• Dayang Chem (Hangzhou) Co.,Ltd.
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• 2-Aziridinone,1,3-bis(1,1-dimethylethyl)- cas 14387-89-4

  Cas No: 14387-89-4

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• Hangzhou Fandachem Co.,Ltd
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14387-89-4 Usage

Chemical family

Aziridine family

Structure

Cyclic organic compound

Common use

Building block in organic synthesis

Application

Production of pharmaceuticals and agrochemicals

Reactivity

Known for its reactivity and ability to undergo various chemical reactions

Versatility

Versatile intermediate in the synthesis of complex organic molecules

Potential use

Development of new materials

Chirality

Chiral building block for asymmetric synthesis

Safety

Handle with caution and follow proper safety procedures and guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 14387-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,8 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14387-89:
(7*1)+(6*4)+(5*3)+(4*8)+(3*7)+(2*8)+(1*9)=124
124 % 10 = 4
So 14387-89-4 is a valid CAS Registry Number.

InChI:InChI=1/C10H19NO/c1-9(2,3)7-8(12)11(7)10(4,5)6/h7H,1-6H3

14387-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	1,3-Di-tert-butylaziridinone

1.2 Other means of identification

Product number	-
Other names	1,3-ditert-butyl-2-aziridinone

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:14387-89-4 SDS

14387-89-4Upstream product

• 14387-96-3 2-bromo-N-(tert-butyl)-3,3-dimethylbutanamide 

14387-89-4Downstream Products

• 60294-85-1 2-tert-butylamino-3,3-dimethyl-1-phenyl-1-butanone 
• 91076-36-7 N-(2,2-Dimethylpropylidene)-1,1-dimethylethanamin 

14387-89-4Relevant articles and documents

Rhodium-catalyzed coupling of α-lactams with indole derivatives

Box, Hannah K.,Upul Kumarasinghe,Nareddy, Radhika R.,Akurathi, Gopalakrishna,Chakraborty, Amarraj,Raji, Babatunde,Rowland, Gerald B.

, p. 9709 - 9717 (2015/02/02)

We report herein a method that allows for the formation of a C-N bond between the C-3 carbon of α-lactams and the nitrogen atom of indoles. A general procedure for the coupling of indoles and α-lactams in only 25 min with high yield is reported. The scope of the reaction was extended by the development of a method for the in situ generation of less stable phenyl-substituted α-lactams. The developed method provides an atom-economical method for the formation of substituted α-amino amides that are found in a variety of biologically-active compounds.

About the factors which govern the ring-opening of α-lactams with benzylamine: I. The relative stability of the α-lactam and the substituent on nitrogen

Lengyel, Istvan,Cesare, Victor,Chen, Sihao,Taldone, Tony

, p. 677 - 695 (2007/10/03)

Eight α-lactams (aziridinones) of varying stability, one of them previously unreported, were synthesized and reacted with benzylamine. Three of the α-lactams, 1-(1-adamantyl)-3,3-dimethylaziridinone (2j), 3,3-dimethyl1-triphenylmethylaziridinone (2m), and

Phase-Transfer-Catalyzed Reactions of α-Haloamides: Synthesis of α-Lactams

Scrimin, Paolo,D'Angeli, Ferruccio,Veronese, Augusto C.

, p. 586 - 587 (2007/10/02)

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