Welcome to LookChem.com Sign In|Join Free
  • or
2-Cyclohexen-1-one, 2-[(5,5-dimethyl-3-oxo-1-cyclohexen-1-yl)oxy]-3-methoxy-5,5-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88089-23-0

Post Buying Request

88089-23-0 Suppliers

Recommended suppliers

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

88089-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88089-23-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,8 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88089-23:
(7*8)+(6*8)+(5*0)+(4*8)+(3*9)+(2*2)+(1*3)=170
170 % 10 = 0
So 88089-23-0 is a valid CAS Registry Number.

88089-23-0SDS

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 3-methoxy-5,5-dimethyl-2-(5,5-dimethyl-3-oxo-1-cyclohexenyl)-2-cyclohexenone

1.2 Other means of identification

Product number -
Other names 2-(5,5-Dimethyl-3-oxo-cyclohex-1-enyloxy)-3-methoxy-5,5-dimethyl-cyclohex-2-enone

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:88089-23-0 SDS

88089-23-0Downstream Products

88089-23-0Relevant academic research and scientific papers

THE PRODUCT FROM THE REACTION OF DIAZOMETHANE WITH 1,3-OXASELENOLE DERIVED FROM DIMEDONE

Matoba, Katsuhide,Yamazaki, Takao

, p. 1959 - 1962 (2007/10/02)

The 1,3-oxaselenole derivative (VI) obtained from dimedone was treated with an excess of diazomethane to give 1,4,7-dioxaselenocine derivative (VII) in a quantitative yield.The deselenization of VII was carried out by the benzyne-hydrogenolysis method to give 3-methoxy-5,5-dimethyl-2-(5,5-dimethyl-3-oxo-1-cyclohexen-1-yl)oxy-2-cyclohexenone (VIII).Treatment of VII with aqueous alkali gave 5,5,5',5'-tetramethyl-1,1',3,3'-tetroxo-2,2'-cyclohexylmethane (IX), and it afforded 4,4'-dibromo-3,3-dimethoxy-5,5-dimethylcyclohexanone (X) with bromine in MeOH.VII was reduced sodium borohydride to an allyl alcohol (XIa) which was converted to its acetate (XIb).

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 88089-23-0