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Cycloheptylacetic acid, with the chemical formula C8H14O2, is a carboxylic acid featuring a seven-carbon cycloalkane ring structure. This white crystalline solid is slightly soluble in water and serves as a versatile precursor in the synthesis of pharmaceuticals and agrochemicals. Its potential anti-inflammatory and analgesic properties have attracted attention for drug development, while its potential use in polymer and plastic production highlights its multifaceted applications across various industries.

4401-20-1

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4401-20-1 Usage

Uses

Used in Pharmaceutical Industry:
Cycloheptylacetic acid is used as a precursor in the synthesis of pharmaceuticals for its potential anti-inflammatory and analgesic properties, making it a target for drug development aimed at treating various inflammatory and pain-related conditions.
Used in Agrochemical Industry:
In the agrochemical sector, cycloheptylacetic acid is utilized as a starting material for the production of agrochemicals, contributing to the development of new compounds for agricultural applications.
Used in Materials Industry:
Cycloheptylacetic acid is employed in the production of various polymers and plastics, showcasing its potential in enhancing material properties and expanding the range of applications in the materials industry.

Check Digit Verification of cas no

The CAS Registry Mumber 4401-20-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,0 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4401-20:
(6*4)+(5*4)+(4*0)+(3*1)+(2*2)+(1*0)=51
51 % 10 = 1
So 4401-20-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c10-9(11)7-8-5-3-1-2-4-6-8/h8H,1-7H2,(H,10,11)

4401-20-1 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L15553)  Cycloheptylacetic acid, 99%   

  • 4401-20-1

  • 1g

  • 683.0CNY

  • Detail
  • Alfa Aesar

  • (L15553)  Cycloheptylacetic acid, 99%   

  • 4401-20-1

  • 5g

  • 2624.0CNY

  • Detail

4401-20-1SDS

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 Cycloheptylacetic Acid

1.2 Other means of identification

Product number -
Other names 2-Cycloheptylacetic 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:4401-20-1 SDS

4401-20-1Relevant academic research and scientific papers

Unusual products from dirhodium tetraacetylate-catalyzed decomposition of diazoacetylcycloalkanes

Ceccherelli, Paolo,Curini, Massimo,Marcotullio, Maria Carla,Pisani, Emanuela,Rosati, Ornelio,Wenkert, Ernest

, p. 8501 - 8506 (2007/10/03)

Rh2(OAc)4-assisted decompositions of diazoacetylcycloalkanes are shown to yield cycloalkylacetic acids (Wolff rearrangement), unexpected cycloalkylcarboxylic acids and bicyclic ketones (intramolecular C-H bond insertion). Rh2(OCOF3)4-promoted reactions, on the other hand, have furnished bicyclic ketones and ketene dimers.

POTENTIAL CEREBRAL STIMULANTS: ESTERS OF 2-DIMETHYLAMINOETHANOL WITH SOME LIPOPHILIC CARBOXYLIC ACIDS

Protiva, Miroslav,Valenta, Vladimir,Kopicova, Zdenka,Lukac, Juraj,Holubek, Jiri,Krejci, Ivan

, p. 1278 - 1289 (2007/10/02)

2-Dimethylaminoethyl esters of 2,2-dimethylpropanoic, heptanoic, octanoic, decanoic, hexadecanoic, cyclopentylacetic, cycloheptylacetic, 2-cyclopenthylhexanoic, (4-chlorophenoxy)fumaric, and 2-(4-chlorophenoxy)succinic acid were prepared by reactions of the acid chlorides with 2-dimethylaminoethanol and were transformed to crystalline salts for pharmacological testing.The ester IX (hydrogen fumarate VUFB-14005) was found to antagonize significantly halothan amnesia in rats and the ester X (hydrogen fumarate VUFB-14004) proved to be an anticholinergic spasmolytic agent.

Dicarboxylic acids and derivatives

-

, (2008/06/13)

Benzocycloalkenderivatives substituted in 1-position by carboxyl and carboxyalkyl or two carboxyl groups, and further substituted in the benzene ring by cycloalkyl and optionally other substituents, their esters, amides and pharmaceutically acceptable sal

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