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64779-07-3

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64779-07-3 Usage

General Description

4-OXO-4-(4-PENTYLPHENYL)BUTANOIC ACID is a chemical compound that belongs to the class of carboxylic acids. It consists of a butanoic acid core with a 4-oxo-4-(4-pentylphenyl) group attached to it. 4-OXO-4-(4-PENTYLPHENYL)BUTANOIC ACID has potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science. It may also possess biological activities and could be of interest for further study in drug development and medicinal chemistry. Its specific properties and potential uses would need to be further investigated through research and experimentation.

Check Digit Verification of cas no

The CAS Registry Mumber 64779-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,7 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64779-07:
(7*6)+(6*4)+(5*7)+(4*7)+(3*9)+(2*0)+(1*7)=163
163 % 10 = 3
So 64779-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O3/c1-2-3-4-5-12-6-8-13(9-7-12)14(16)10-11-15(17)18/h6-9H,2-5,10-11H2,1H3,(H,17,18)

64779-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-OXO-4-(4-PENTYLPHENYL)BUTANOIC ACID

1.2 Other means of identification

Product number -
Other names HMS547A02

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:64779-07-3 SDS

64779-07-3Downstream Products

64779-07-3Relevant articles and documents

Alkylarylketo acids

-

, (2008/06/13)

Disclosed are novel alkylarylketocarboxylic acids and 5-substituted tetrazoles represented by the formula STR1 wherein Z is aryl or an alkyl of the structure STR2 W is a carboxyl moiety or a tetrazole moiety bound to Z at the 5-position of the tetrazole; R1 is C4 -C12 alkyl where Z is aryl and X is oxygen or is C5 -C12 alkyl where Z is alkyl and where Z is aryl and X is a bond; R2 and R3 are each independently hydrogen, C1 -C4 alkyl, hydroxy, C1 -C4 alkoxy, halogen, trihalomethyl, nitro, cyano or C1 -C4 acyl; R4, R5, R6 and R7 are each independently hydrogen or C1 -C4 alkyl or R4 and R6 or R5 and R7 can combine to form a carbocyclic ring; X is oxygen, or a bond at the ortho or para position; m is 0, 1 or 2; and n is 0 or 1, and nontoxic, pharmaceutically acceptable addition salts and carboxylic acid esters thereof.

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