Welcome to LookChem.com Sign In|Join Free
  • or
3,5-Cyclohexadiene-1,2-dione, 4,6-bis(diphenylmethyl)-3-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

212055-89-5

Post Buying Request

212055-89-5 Suppliers

Recommended suppliers

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

212055-89-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 212055-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,0,5 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 212055-89:
(8*2)+(7*1)+(6*2)+(5*0)+(4*5)+(3*5)+(2*8)+(1*9)=95
95 % 10 = 5
So 212055-89-5 is a valid CAS Registry Number.

212055-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dibenzhydryl-3-methoxycyclohexa-3,5-diene-1,2-dione

1.2 Other means of identification

Product number -
Other names -

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:212055-89-5 SDS

212055-89-5Relevant academic research and scientific papers

SnCl4-catalyzed reaction of o-benzoquinones and aryl acetylenes: An unprecedented one-pot synthesis of tropone derivatives

Nair, Vijay,Sethumadhavan,Nair, Smitha M.,Rath, Nigam P.,Eigendorf, Guenter K.

, p. 7533 - 7536 (2002)

Highly substituted tropone derivatives were obtained as a result of SnCl4-catalyzed cycloaddition of 3-methoxy-substituted o-benzoquinones with aryl acetylenes and subsequent rearrangement of the adducts with concomitant decarbonylation.

Efficient Diels-Alder reaction of 1,2-benzoquinones with arynes and its utility in one-pot reactions

Kaicharla, Trinadh,Bhojgude, Sachin Suresh,Biju, Akkattu T.

supporting information, p. 6238 - 6241 (2013/02/25)

A new protocol for the efficient Diels-Alder reaction of 1,2-benzoquinones with arynes is reported. The aryne generated by the fluoride-induced 1,2-elimination of 2-(trimethylsilyl)aryl triflates undergoes a facile Diels-Alder reaction with 1,2-benzoquinones, affording the dioxobenzobicyclooctadienes in moderate to excellent yields. In addition, this methodology has been applied to the one-pot synthesis of benzoquinoxalinobarrelene and naphthalene derivatives.

Reaction of huisgen zwitterion with 1,2-benzoquinones and isatins: Expeditious synthesis of dihydro-1,2,3-benzoxadiazoles and spirooxadiazolines

Nair, Vijay,Biju,Vinod,Suresh, Eringathodi

, p. 5139 - 5142 (2007/10/03)

(Chemical Equation Presented) The zwitterionic intermediate generated from dialkyl azodicarboxylate and triphenylphosphine on reaction with 3-methoxy-1,2-benzoquinones afforded dihydro-1,2,3-benzoxadiazoles. N-Substituted isatins furnished spirooxadiazoli

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 212055-89-5