154881-54-6

• 

• Basic information

  1. Product Name: Ethanone, 1-(2-phenyloxiranyl)- (9CI)
  2. Synonyms: Ethanone, 1-(2-phenyloxiranyl)- (9CI)
  3. CAS NO:154881-54-6
  4. Molecular Formula: C₁₀H₁₀O₂
  5. Molecular Weight: 162.1852
  6. EINECS: N/A
  7. Product Categories: ACETYLGROUP
  8. Mol File: 154881-54-6.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Ethanone, 1-(2-phenyloxiranyl)- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Ethanone, 1-(2-phenyloxiranyl)- (9CI)(154881-54-6)
  11. EPA Substance Registry System: Ethanone, 1-(2-phenyloxiranyl)- (9CI)(154881-54-6)

• 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: 154881-54-6(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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154881-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154881-54-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,8,8 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 154881-54:
(8*1)+(7*5)+(6*4)+(5*8)+(4*8)+(3*1)+(2*5)+(1*4)=156
156 % 10 = 6
So 154881-54-6 is a valid CAS Registry Number.

154881-54-6SDS

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-acetyl-2-phenyloxirane

1.2 Other means of identification

Product number	-
Other names	1-(2-Phenyl-oxiranyl)-ethanone

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:154881-54-6 SDS

154881-54-6Upstream product

• 62-53-3 aniline 
• 103-79-7 1-phenyl-acetone 
• 31034-99-8 4-dimethylamino-3-phenyl-2-butanone methiodide 
• 32123-84-5 3-phenylbut-3-en-2-one 

154881-54-6Downstream Products

• 154881-47-7 4-methyl-5-dimethylaminomethyl-5-phenyl-2(5H)-furanone 
• 204516-17-6 2,3-dihydro-3-hydroxy-3-phenyl-6-(trifluoromethyl)-4H-pyran-4-one 
• 108272-47-5 3-hydroxy-4-dimethylamino-3-phenyl-2-butanone 
• 204516-29-0 3-Chloro-3-phenyl-6-trifluoromethyl-2,3-dihydro-pyran-4-one 
• 204516-20-1 5-phenyl-2-(trifluoromethyl)-4H-pyran-4-one 

154881-54-6Relevant articles and documents

Asymmetric Catalytic Epoxidation of Terminal Enones for the Synthesis of Triazole Antifungal Agents

Feng, Xiaoming,He, Qianwen,Liu, Xiaohua,Zhang, Dong,Zhang, Fengcai

, p. 6961 - 6966 (2021/09/11)

An enantioselective epoxidation of α-substituted vinyl ketones was realized to construct the key epoxide intermediates for the synthesis of various triazole antifungal agents. The reaction proceeded efficiently in high yields with good enantioselectivities by employing a chiral N,N′-dioxide/ScIII complex as the chiral catalyst and 35% aq. H2O2 as the oxidant. It enabled the facile transformation for optically active isavuconazole, efinaconazole, and other potential antifungal agents.

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