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5454-78-4

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5454-78-4 Usage

General Description

2-methylcyclopentane-1-carboxylic acid is a chemical compound with the molecular formula C8H14O2. It is a carboxylic acid, meaning it contains a carboxyl functional group, and is derived from cyclopentane with a methyl group attached at the 2 position. 2-methylcyclopentane-1-carboxylic acid is used in organic synthesis and pharmaceutical research due to its unique structural features and potential biological activity. It may also have applications in the development of new materials and in the production of flavors and fragrances. Overall, 2-methylcyclopentane-1-carboxylic acid has the potential to be a valuable building block in various chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 5454-78-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5454-78:
(6*5)+(5*4)+(4*5)+(3*4)+(2*7)+(1*8)=104
104 % 10 = 4
So 5454-78-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-5-3-2-4-6(5)7(8)9/h5-6H,2-4H2,1H3,(H,8,9)

5454-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylcyclopentane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-methylcyclopentanecarboxylic 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:5454-78-4 SDS

5454-78-4Relevant articles and documents

(Lig)Ni(0) induced preparation of mono- and dicarboxylic acids from cyclopentene and carbon dioxide

Hoberg,Ballesteros,Sigan,Jegat,Milchereit

, p. 395 - 398 (2007/10/02)

Cyclopentene is shown to be an ideal substrate for coupling reactions with (Lig)nickel(0) systems. By variation of the ligands and addition of promoters, it is possible by successive application of carbon dioxide or carbon monoxide to prepare highly selectively series of cyclopentane- and cyclopentenecarboxylic acids (six examples), 4, 5, 6, 11, 14, 15, cyclopentanedicarboxylic acids (three examples), 7, 8, 12, or 2-hydroxycyclopentanecarboxylic acid (9) in good yields. The C5-skeleton is retained in the products.

STEREOCHEMISTRY OF THE HYDROGENOLYSIS OF 1,2-DISUBSTITUTED FERROCENES IN ACID MEDIA

Sokolov, V. I.,Filippova, T. M.,Khrushcheva, N. S.,Troitskaya, L. L.

, p. 2385 - 2387 (2007/10/02)

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