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(3aS,7aS)-1-oxo-1,4,7,7a-tetrahydro-3aH-4,7-ethanoindene-3a-carboxylic acid is a carboxylic acid compound with a molecular formula C11H12O3. It is a cyclic compound with a carboxylic acid functional group, and it is classified as a carboxylic acid.

56689-13-5

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56689-13-5 Usage

Uses

Used in Pharmaceutical Industry:
(3aS,7aS)-1-oxo-1,4,7,7a-tetrahydro-3aH-4,7-ethanoindene-3a-carboxylic acid is used as a synthetic intermediate for the production of various pharmaceuticals and organic compounds. Its unique structure and properties make it a valuable building block for the synthesis of other complex organic molecules.
Used in Medicinal Chemistry and Drug Development:
(3aS,7aS)-1-oxo-1,4,7,7a-tetrahydro-3aH-4,7-ethanoindene-3a-carboxylic acid has potential applications in medicinal chemistry and drug development due to its unique structure and properties. It can be used to develop new drugs and improve existing ones.
Overall, (3aS,7aS)-1-oxo-1,4,7,7a-tetrahydro-3aH-4,7-ethanoindene-3a-carboxylic acid has important industrial and scientific uses.

Check Digit Verification of cas no

The CAS Registry Mumber 56689-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,8 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56689-13:
(7*5)+(6*6)+(5*6)+(4*8)+(3*9)+(2*1)+(1*3)=165
165 % 10 = 5
So 56689-13-5 is a valid CAS Registry Number.

56689-13-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name NSC329356

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:56689-13-5 SDS

56689-13-5Downstream Products

56689-13-5Relevant academic research and scientific papers

SYNTHESIS AND -CYCLOREVERSION OF CAGE KETONES

Yamashita, Yoshiro,Mukai, Toshio

, p. 1741 - 1744 (2007/10/02)

A series of pentacyclic cage ketones 2b-d having no substituent was synthesized by the photochemical -cycloaddition reaction of corresponding tricyclic dienones 1b-d.The cage ketones 2b-d underwent thermal -cycloreversion to give dienones 1b-d.The reactivities were dependent on the length of the bridge "X".

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