Welcome to LookChem.com Sign In|Join Free
  • or
Oxirane, 2-(4-fluorophenyl)-3-methyl-, (2R,3S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

403501-33-7

Post Buying Request

403501-33-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

403501-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403501-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,5,0 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 403501-33:
(8*4)+(7*0)+(6*3)+(5*5)+(4*0)+(3*1)+(2*3)+(1*3)=87
87 % 10 = 7
So 403501-33-7 is a valid CAS Registry Number.

403501-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2S)-1-(4-fluorophenyl)-1-propene oxide

1.2 Other means of identification

Product number -
Other names (2R,3S)-2-(4-Fluoro-phenyl)-3-methyl-oxirane

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:403501-33-7 SDS

403501-33-7Downstream Products

403501-33-7Relevant academic research and scientific papers

Asymmetric epoxidation of cis-β-methylstyrenes catalyzed by N-aryl substituted oxazolidinone-containing ketones. A beneficial substituent effect

Shu, Lianhe,Shi, Yian

, p. 8115 - 8117 (2007/10/03)

Asymmetric epoxidation of substituted cis-β-methylstyrenes using N-aryl substituted oxazolidinone-containing ketones as catalysts shows that substituents on the phenyl group of the olefin have significant positive effects on the enantioselectivity of the

Designing new chiral ketone catalysts. Asymmetric epoxidation of cis-olefins and terminal olefins

Tian, Hongqi,She, Xuegong,Yu, Hongwu,Shu, Lianhe,Shi, Yian

, p. 2435 - 2446 (2007/10/03)

This paper describes a new class of chiral oxazolidinone ketone catalyst for asymmetric epoxidation. High ee values have been obtained for a number of cyclic and acyclic cis-olefins. The epoxidation was stereospecific with no isomerization observed in the epoxidation of acyclic systems. Encouragingly high ee values have also been obtained for a number of terminal olefins. Mechanistic studies show that electronic interactions play an important role in stereodifferentiation.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 403501-33-7