Welcome to LookChem.com Sign In|Join Free
  • or
2-Octenoic acid, 4-hydroxy-7-oxo-, phenylmethyl ester, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

918343-89-2

Post Buying Request

918343-89-2 Suppliers

Recommended suppliers

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

918343-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918343-89-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,3,4 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 918343-89:
(8*9)+(7*1)+(6*8)+(5*3)+(4*4)+(3*3)+(2*8)+(1*9)=192
192 % 10 = 2
So 918343-89-2 is a valid CAS Registry Number.

918343-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 4-hydroxy-7-oxooct-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Octenoic acid,4-hydroxy-7-oxo-,phenylmethyl ester,(2E)

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:918343-89-2 SDS

918343-89-2Downstream Products

918343-89-2Relevant academic research and scientific papers

A facile access to bridged 1,2,4-trioxanes

Zhang, Qi,Jin, Hong-Xia,Wu, Yikang

, p. 11627 - 11634 (2007/10/03)

Bicyclo[3.2.1] type 1,2,4-trioxanes are readily synthesized from precursors that may form intramolecular hemiketals using UHP (H2O2-urea complex) as the source of the peroxy bond and p-TsOH or CSA as the catalyst. The ring closure through an intramolecular Michael addition occurred in a highly stereoselective way, giving only one diasteromer as shown by the NMR spectra.

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 918343-89-2