Welcome to LookChem.com Sign In|Join Free
  • or
7-Oxabicyclo[4.1.0]heptane-2-aceticacid,4-hydroxy-1-methyl-,methylester,(1R,2S,4R,6S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

744207-92-9

Post Buying Request

744207-92-9 Suppliers

Recommended suppliers

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

744207-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 744207-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,4,2,0 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 744207-92:
(8*7)+(7*4)+(6*4)+(5*2)+(4*0)+(3*7)+(2*9)+(1*2)=159
159 % 10 = 9
So 744207-92-9 is a valid CAS Registry Number.

744207-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2S,4R,6S)-[4-hydroxy-1-methyl-7-oxabicyclo[4.1.0]hept-2-yl]acetic acid methyl ester

1.2 Other means of identification

Product number -
Other names ((1R,2S,4R,6S)-4-Hydroxy-1-methyl-7-oxa-bicyclo[4.1.0]hept-2-yl)-acetic acid methyl ester

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:744207-92-9 SDS

744207-92-9Downstream Products

744207-92-9Relevant academic research and scientific papers

Cp2TiCl-promoted isomerization of trisubstituted epoxides to exo-methylene allylic alcohols on carvone derivatives

Bermejo, Francisco,Sandoval, Celso

, p. 5275 - 5280 (2007/10/03)

The ring-opening reaction of trisubstituted epoxides promoted by Cp 2TiCl led to exo-methylene allylic alcohols as major compounds when 0.5 M solutions of the epoxides were added to 0.1 M solutions of the reagent at room temperature in THF. In most cases, the allylic alcohols were contaminated with saturated alcohols. Normal and reverse addition modes led to the alternate product being favored. The different stereochemical outcome of cis- and trans-epoxy acetates is rationalized in terms of mechanistically biased elimination processes.

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 744207-92-9