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4a(2H)-Naphthalenecarboxylic acid, octahydro-, also known as decahydro-4a-naphthoic acid, is a chemical compound with the molecular formula C11H16O2. It is a white crystalline solid that belongs to the class of naphthalene derivatives. 4a(2H)-Naphthalenecarboxylic acid, octahydro- is characterized by its bicyclic structure, with a naphthalene ring fused to a cyclohexane ring, and a carboxylic acid functional group attached to the 4a position. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. The compound is typically synthesized through various chemical reactions, such as the reduction of naphthalene derivatives or the cyclization of linear precursors. Due to its unique structure and reactivity, it has potential applications in the development of new drugs and materials.

7112-20-1

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7112-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7112-20-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,1 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7112-20:
(6*7)+(5*1)+(4*1)+(3*2)+(2*2)+(1*0)=61
61 % 10 = 1
So 7112-20-1 is a valid CAS Registry Number.

7112-20-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cis/trans-decahydronaphthalene-4a-carboxylic acid

1.2 Other means of identification

Product number -
Other names Decalin-9-carbonsaeure

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:7112-20-1 SDS

7112-20-1Downstream Products

7112-20-1Relevant academic research and scientific papers

Regio- and stereoselective acylation of saturated carbocycles via Norrish-Yang photocyclization

Kamijo, Shin,Hoshikawa, Tamaki,Inoue, Masayuki

supporting information; experimental part, p. 872 - 874 (2010/03/26)

A regio- and stereoselective acylation of saturated carbocycles has been achieved through two-step reactions involving the Norrish-Yang photocyclization of 1,2-diketones and subsequent ring opening of the α-hydroxy-cyclobutanones. The C-H activation of the carbocycle proceeds regioselectively at vicinal to the diketone moiety resulting in stereoselective formation of cis-fused bicycles. The following C-C cleavage affords vicinally cis-acylated carbocycles. Predictability, generality, and practicality of the present strategy have been demonstrated using variously modified saturated carbocycles.

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