Welcome to LookChem.com Sign In|Join Free
  • or
Bicyclo[2.2.2]octane-7,8-dicarboxylic acid is a cyclic organic compound with the molecular formula C10H12O4. It features a bicyclic structure, where two carbon rings are fused together, with the second ring being a smaller three-membered ring. The compound has two carboxylic acid functional groups attached to the seventh and eighth carbon atoms of the bicyclic structure. This unique arrangement of atoms and functional groups endows bicyclo[2.2.2]octane-7,8-dicarboxylic acid with specific chemical properties and reactivity, making it a potentially useful building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its stability, solubility, and ability to form derivatives through chemical reactions are some of the factors that make it an interesting compound for further exploration in the field of organic chemistry.

6303-66-8

Post Buying Request

6303-66-8 Suppliers

Recommended suppliers

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

6303-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6303-66-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6303-66:
(6*6)+(5*3)+(4*0)+(3*3)+(2*6)+(1*6)=78
78 % 10 = 8
So 6303-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O4/c11-9(12)7-5-1-2-6(4-3-5)8(7)10(13)14/h5-8H,1-4H2,(H,11,12)(H,13,14)

6303-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[2.2.2]octane-2,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names trans-2,3-Dicarboxybicyclo<2.2.2>octan

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:6303-66-8 SDS

6303-66-8Downstream Products

6303-66-8Relevant academic research and scientific papers

Enzymatic optical resolution of norbornanecarboxylic esters using Pig Liver Esterase

Gastel, F. J. C. van,Klunder, A. J. H.,Zwanenburg, B.

, p. 175 - 184 (2007/10/02)

The hydrolysis of a series of norbornane-type carboxylic esters catalyzed by pig liver esterase (PLE) has been investigated.It was found that an exo-ester function (syn to the C7 methylene group) is hydrolyzed with high preference.Enantioselective hydrolysis can be accomplished when a vicinal carbonyl-containing function (ester, formyl, acetyl) is present in a trans position with respect to the exo ester.The regiospecifity of the enzymatic hydrolysis has been used for the separation of exo/endo mixtures of the cycloadducts derived from cyclopentadiene and alkene esters.The regiospecifity and enantioselectivity of the enzymatic hydrolysis of norbornane-type esters were analyzed in terms of Tamm's substrate model and also by Griengl's method.

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 6303-66-8