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Cyclohexaneoctanoic acid, also known as 1-cyclohexaneoctanoic acid or cyclohexanecarboxylic acid, is an organic compound with the chemical formula C12H22O2. It features a cyclohexane ring fused to an octanoic acid chain, which consists of a six-carbon cyclohexane ring and an eight-carbon aliphatic chain with a carboxylic acid group at the end. Cyclohexaneoctanoic acid is a white crystalline solid with a melting point of approximately 40-42°C. Cyclohexaneoctanoic acid is used in various applications, including the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential use as a chiral building block in the production of enantiomerically pure compounds.

4352-56-1

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4352-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4352-56-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4352-56:
(6*4)+(5*3)+(4*5)+(3*2)+(2*5)+(1*6)=81
81 % 10 = 1
So 4352-56-1 is a valid CAS Registry Number.

4352-56-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-cyclohexyloctanoic acid

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:4352-56-1 SDS

4352-56-1Relevant academic research and scientific papers

Nickel-butadiene catalytic system for the cross-coupling of bromoalkanoic acids with alkyl grignard reagents: A practical and versatile method for preparing fatty acids

Iwasaki, Takanori,Higashikawa, Kiyokazu,Reddy, Vutukuri P.,Ho, Willbe W. S.,Fujimoto, Yukari,Fukase, Koichi,Terao, Jun,Kuniyasu, Hitoshi,Kambe, Nobuaki

supporting information, p. 2956 - 2960 (2013/03/28)

The knights who say Ni: A practical and convenient synthetic route to fatty acids involves the Ni-catalyzed alkyl-alkyl cross-coupling of bromoalkanoic acids and alkyl Grignard reagents in the presence of 1,3-butadiene as an additive (see scheme). Copyright

7-oxabicycloheptyl substituted heterocyclic amide or ester prostaglandin analogs useful in the treatment of thrombotic and vasospastic disease

-

, (2008/06/13)

7-Oxabicycloheptane substituted prostaglandin analogs useful in treating thrombotic and vasopastic disease have the structural formula STR1 wherein m is 1, 2 or 3; n is 1, 2, 3 or 4; Z is --(CH2)2 --, --CH=CH-- or STR2 wherein Y is O, a single bond or vinyl, with the proviso that when n is 0, if Z is STR3 then Y cannot be O, and Z is --CH=CH--, n is 1, 2, 3 or 4; and when Y=vinyl, n=0; R is CO2 H, CO2 lower alkyl, CH2 OH, CO2 alkali metal, CONHSOR3, CONHR3a or --CH2 --5-tetrazolyl, X is O, S or NH; and where R1, R2, R3 and R3a are as defined herein.

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