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Cis-octahydro-4a(2H)-naphthalenecarboxylic acid is a chemical compound with the molecular formula C11H14O3. It is a white crystalline solid that belongs to the class of organic compounds known as naphthalene derivatives. CIS-OCTAHYDRO-4A(2H)-NAPHTHALENECARBOXYLIC ACID is characterized by its unique cis-octahydro structure, which consists of a saturated eight-membered ring fused to a naphthalene core. The molecule features a carboxylic acid functional group, which is responsible for its acidic properties. Cis-octahydro-4a(2H)-naphthalenecarboxylic acid has potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.

3021-73-6

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3021-73-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3021-73-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,2 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3021-73:
(6*3)+(5*0)+(4*2)+(3*1)+(2*7)+(1*3)=46
46 % 10 = 6
So 3021-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O2/c12-10(13)11-7-3-1-5-9(11)6-2-4-8-11/h9H,1-8H2,(H,12,13)

3021-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-decalin-9-carboxylic acid

1.2 Other means of identification

Product number -
Other names Octahydro-naphthalene-4a-carboxylic acid

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:3021-73-6 SDS

3021-73-6Downstream Products

3021-73-6Relevant academic research and scientific papers

Studies in Alicyclic Compounds: Part VII - Koch-Haaf Carboxylation of 1-Cycloalkylcycloalkanols

Rao, R. R.,Bhattacharya, S.

, p. 207 - 209 (2007/10/02)

The Koch-Haaf carboxylation (K-H-C) of 1-cycloalkylcyclopentanols (Ia and Ib) and 1-cycloalkylcyclohexanols (VIa and VIb) has been investigated.In the case of 1-cycloalkylcyclopentanols (Ia and Ib), K-H-C results in the formation of rearranged tertiary (30) bridgehead acids (Va and Vb) providing interesting examples of ring expansion reactions, whereas K-H-C of 1-cycloalkylcyclohexanols (VIa and VIb) furnishes the corresponding 30 carboxylic acids (VIIIa and VIIIb) in good yields.

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